Canonical Allele Identifier: CA1260120279

Gene: DYSF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71602933_71602936delinsTCTG , CM000664.2:g.71602933_71602936delinsTCTG	GRCh38
NC_000002.11:g.71830063_71830066delinsTCTG , CM000664.1:g.71830063_71830066delinsTCTG	GRCh37
NC_000002.10:g.71683571_71683574delinsTCTG	NCBI36
NG_008694.1:g.154311_154314delinsTCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.1329+128_1329+131delinsTCTG	ENSP00000513536.1:n.1329+128_1329+131delinsTCTG
ENST00000698058.1:c.546+128_546+131delinsTCTG	ENSP00000513537.1:n.546+128_546+131delinsTCTG
ENST00000698059.1:c.546+128_546+131delinsTCTG	ENSP00000513538.1:n.546+128_546+131delinsTCTG
ENST00000258104.8:c.3903+128_3903+131delinsTCTG MANE Plus Clinical	ENSP00000258104.3:n.3903+128_3903+131delinsTCTG
ENST00000410020.8:c.3957+128_3957+131delinsTCTG MANE Select	ENSP00000386881.3:n.3957+128_3957+131delinsTCTG
ENST00000258104.7:c.3903+128_3903+131delinsTCTG	ENSP00000258104.3:n.3903+128_3903+131delinsTCTG
ENST00000394120.6:c.3906+128_3906+131delinsTCTG	ENSP00000377678.2:n.3906+128_3906+131delinsTCTG
ENST00000409366.5:c.3906+128_3906+131delinsTCTG	ENSP00000386512.1:n.3906+128_3906+131delinsTCTG
ENST00000409582.7:c.3954+128_3954+131delinsTCTG	ENSP00000386547.3:n.3954+128_3954+131delinsTCTG
ENST00000409651.5:c.3999+128_3999+131delinsTCTG	ENSP00000386683.1:n.3999+128_3999+131delinsTCTG
ENST00000409744.5:c.3864+128_3864+131delinsTCTG	ENSP00000386285.1:n.3864+128_3864+131delinsTCTG
ENST00000409762.5:c.3954+128_3954+131delinsTCTG	ENSP00000387137.1:n.3954+128_3954+131delinsTCTG
ENST00000410020.7:c.3957+128_3957+131delinsTCTG	ENSP00000386881.3:n.3957+128_3957+131delinsTCTG
ENST00000410041.1:c.3957+128_3957+131delinsTCTG	ENSP00000386617.1:n.3957+128_3957+131delinsTCTG
ENST00000413539.6:c.3996+128_3996+131delinsTCTG	ENSP00000407046.2:n.3996+128_3996+131delinsTCTG
ENST00000429174.6:c.3903+128_3903+131delinsTCTG	ENSP00000398305.2:n.3903+128_3903+131delinsTCTG
ENST00000472873.5:n.287+128_287+131delinsTCTG
ENST00000479049.6:n.788+128_788+131delinsTCTG
ENST00000487180.5:n.122+128_122+131delinsTCTG
ENST00000494501.5:n.263+128_263+131delinsTCTG
NM_001130455.1:c.3906+128_3906+131delinsTCTG	NP_001123927.1:n.3906+128_3906+131delinsTCTG
NM_001130976.1:c.3861+128_3861+131delinsTCTG	NP_001124448.1:n.3861+128_3861+131delinsTCTG
NM_001130977.1:c.3861+128_3861+131delinsTCTG	NP_001124449.1:n.3861+128_3861+131delinsTCTG
NM_001130978.1:c.3903+128_3903+131delinsTCTG	NP_001124450.1:n.3903+128_3903+131delinsTCTG
NM_001130979.1:c.3996+128_3996+131delinsTCTG	NP_001124451.1:n.3996+128_3996+131delinsTCTG
NM_001130980.1:c.3954+128_3954+131delinsTCTG	NP_001124452.1:n.3954+128_3954+131delinsTCTG
NM_001130981.1:c.3954+128_3954+131delinsTCTG	NP_001124453.1:n.3954+128_3954+131delinsTCTG
NM_001130982.1:c.3999+128_3999+131delinsTCTG	NP_001124454.1:n.3999+128_3999+131delinsTCTG
NM_001130983.1:c.3906+128_3906+131delinsTCTG	NP_001124455.1:n.3906+128_3906+131delinsTCTG
NM_001130984.1:c.3864+128_3864+131delinsTCTG	NP_001124456.1:n.3864+128_3864+131delinsTCTG
NM_001130985.1:c.3957+128_3957+131delinsTCTG	NP_001124457.1:n.3957+128_3957+131delinsTCTG
NM_001130986.1:c.3864+128_3864+131delinsTCTG	NP_001124458.1:n.3864+128_3864+131delinsTCTG
NM_001130987.1:c.3957+128_3957+131delinsTCTG	NP_001124459.1:n.3957+128_3957+131delinsTCTG
NM_003494.3:c.3903+128_3903+131delinsTCTG	NP_003485.1:n.3903+128_3903+131delinsTCTG
XM_005264584.3:c.3999+128_3999+131delinsTCTG	XP_005264641.1:n.3999+128_3999+131delinsTCTG
XM_005264585.3:c.3996+128_3996+131delinsTCTG	XP_005264642.1:n.3996+128_3996+131delinsTCTG
XM_005264584.4:c.3999+128_3999+131delinsTCTG	XP_005264641.1:n.3999+128_3999+131delinsTCTG
XM_005264585.5:c.3996+128_3996+131delinsTCTG	XP_005264642.1:n.3996+128_3996+131delinsTCTG
XR_001738969.1:n.4157+128_4157+131delinsTCTG
NM_001130987.2:c.3957+128_3957+131delinsTCTG MANE Select	NP_001124459.1:n.3957+128_3957+131delinsTCTG
NM_001130455.2:c.3906+128_3906+131delinsTCTG	NP_001123927.1:n.3906+128_3906+131delinsTCTG
NM_001130976.2:c.3861+128_3861+131delinsTCTG	NP_001124448.1:n.3861+128_3861+131delinsTCTG
NM_001130977.2:c.3861+128_3861+131delinsTCTG	NP_001124449.1:n.3861+128_3861+131delinsTCTG
NM_001130978.2:c.3903+128_3903+131delinsTCTG	NP_001124450.1:n.3903+128_3903+131delinsTCTG
NM_001130979.2:c.3996+128_3996+131delinsTCTG	NP_001124451.1:n.3996+128_3996+131delinsTCTG
NM_001130980.2:c.3954+128_3954+131delinsTCTG	NP_001124452.1:n.3954+128_3954+131delinsTCTG
NM_001130981.2:c.3954+128_3954+131delinsTCTG	NP_001124453.1:n.3954+128_3954+131delinsTCTG
NM_001130982.2:c.3999+128_3999+131delinsTCTG	NP_001124454.1:n.3999+128_3999+131delinsTCTG
NM_001130983.2:c.3906+128_3906+131delinsTCTG	NP_001124455.1:n.3906+128_3906+131delinsTCTG
NM_001130984.2:c.3864+128_3864+131delinsTCTG	NP_001124456.1:n.3864+128_3864+131delinsTCTG
NM_001130985.2:c.3957+128_3957+131delinsTCTG	NP_001124457.1:n.3957+128_3957+131delinsTCTG
NM_001130986.2:c.3864+128_3864+131delinsTCTG	NP_001124458.1:n.3864+128_3864+131delinsTCTG
NM_003494.4:c.3903+128_3903+131delinsTCTG MANE Plus Clinical	NP_003485.1:n.3903+128_3903+131delinsTCTG