Canonical Allele Identifier: CA892689185

Gene: DYSF

Linked Data

• dbSNP Id: rs1472358797
• MyVariant Identifiers: chr2:g.71913372_71913373insA (hg19) ; chr2:g.71686242_71686243insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71686243dup , CM000664.2:g.71686243dup	GRCh38
NC_000002.11:g.71913373dup , CM000664.1:g.71913373dup	GRCh37
NC_000002.10:g.71766881dup	NCBI36
NG_008694.1:g.237621dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.3736-211dup	ENSP00000513536.1:n.3736-211dup
ENST00000698058.1:c.2953-211dup	ENSP00000513537.1:n.2953-211dup
ENST00000698059.1:c.3061-211dup	ENSP00000513538.1:n.3061-211dup
ENST00000258104.8:c.6205-211dup MANE Plus Clinical	ENSP00000258104.3:n.6205-211dup
ENST00000410020.8:c.6322-211dup MANE Select	ENSP00000386881.3:n.6322-211dup
ENST00000258104.7:c.6205-211dup	ENSP00000258104.3:n.6205-211dup
ENST00000394120.6:c.6208-211dup	ENSP00000377678.2:n.6208-211dup
ENST00000409366.5:c.6271-211dup	ENSP00000386512.1:n.6271-211dup
ENST00000409582.7:c.6319-211dup	ENSP00000386547.3:n.6319-211dup
ENST00000409651.5:c.6301-211dup	ENSP00000386683.1:n.6301-211dup
ENST00000409744.5:c.6229-211dup	ENSP00000386285.1:n.6229-211dup
ENST00000409762.5:c.6256-211dup	ENSP00000387137.1:n.6256-211dup
ENST00000410020.7:c.6322-211dup	ENSP00000386881.3:n.6322-211dup
ENST00000410041.1:c.6259-211dup	ENSP00000386617.1:n.6259-211dup
ENST00000413539.6:c.6298-211dup	ENSP00000407046.2:n.6298-211dup
ENST00000429174.6:c.6268-211dup	ENSP00000398305.2:n.6268-211dup
ENST00000479049.6:n.3090-211dup
NM_001130455.1:c.6208-211dup	NP_001123927.1:n.6208-211dup
NM_001130976.1:c.6163-211dup	NP_001124448.1:n.6163-211dup
NM_001130977.1:c.6226-211dup	NP_001124449.1:n.6226-211dup
NM_001130978.1:c.6268-211dup	NP_001124450.1:n.6268-211dup
NM_001130979.1:c.6298-211dup	NP_001124451.1:n.6298-211dup
NM_001130980.1:c.6256-211dup	NP_001124452.1:n.6256-211dup
NM_001130981.1:c.6319-211dup	NP_001124453.1:n.6319-211dup
NM_001130982.1:c.6301-211dup	NP_001124454.1:n.6301-211dup
NM_001130983.1:c.6271-211dup	NP_001124455.1:n.6271-211dup
NM_001130984.1:c.6229-211dup	NP_001124456.1:n.6229-211dup
NM_001130985.1:c.6259-211dup	NP_001124457.1:n.6259-211dup
NM_001130986.1:c.6166-211dup	NP_001124458.1:n.6166-211dup
NM_001130987.1:c.6322-211dup	NP_001124459.1:n.6322-211dup
NM_003494.3:c.6205-211dup	NP_003485.1:n.6205-211dup
XM_005264584.3:c.6364-211dup	XP_005264641.1:n.6364-211dup
XM_005264585.3:c.6361-211dup	XP_005264642.1:n.6361-211dup
XM_005264584.4:c.6364-211dup	XP_005264641.1:n.6364-211dup
XM_005264585.5:c.6361-211dup	XP_005264642.1:n.6361-211dup
NM_001130987.2:c.6322-211dup MANE Select	NP_001124459.1:n.6322-211dup
NM_001130455.2:c.6208-211dup	NP_001123927.1:n.6208-211dup
NM_001130976.2:c.6163-211dup	NP_001124448.1:n.6163-211dup
NM_001130977.2:c.6226-211dup	NP_001124449.1:n.6226-211dup
NM_001130978.2:c.6268-211dup	NP_001124450.1:n.6268-211dup
NM_001130979.2:c.6298-211dup	NP_001124451.1:n.6298-211dup
NM_001130980.2:c.6256-211dup	NP_001124452.1:n.6256-211dup
NM_001130981.2:c.6319-211dup	NP_001124453.1:n.6319-211dup
NM_001130982.2:c.6301-211dup	NP_001124454.1:n.6301-211dup
NM_001130983.2:c.6271-211dup	NP_001124455.1:n.6271-211dup
NM_001130984.2:c.6229-211dup	NP_001124456.1:n.6229-211dup
NM_001130985.2:c.6259-211dup	NP_001124457.1:n.6259-211dup
NM_001130986.2:c.6166-211dup	NP_001124458.1:n.6166-211dup
NM_003494.4:c.6205-211dup MANE Plus Clinical	NP_003485.1:n.6205-211dup