Canonical Allele Identifier: CA1706534

Gene: DYSF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71574337G>A , CM000664.2:g.71574337G>A	GRCh38
NC_000002.11:g.71801467G>A , CM000664.1:g.71801467G>A	GRCh37
NC_000002.10:g.71654975G>A	NCBI36
NG_008694.1:g.125715G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001130987.2:c.3368G>A MANE Select	NP_001124459.1:p.Gly1123Glu
ENST00000410020.8:c.3368G>A MANE Select	ENSP00000386881.3:p.Gly1123Glu
NM_003494.4:c.3314G>A MANE Plus Clinical	NP_003485.1:p.Gly1105Glu
ENST00000258104.8:c.3314G>A MANE Plus Clinical	ENSP00000258104.3:p.Gly1105Glu
NM_001130455.1:c.3317G>A	NP_001123927.1:p.Gly1106Glu
NM_001130455.2:c.3317G>A	NP_001123927.1:p.Gly1106Glu
NM_001130976.1:c.3272G>A	NP_001124448.1:p.Gly1091Glu
NM_001130976.2:c.3272G>A	NP_001124448.1:p.Gly1091Glu
NM_001130977.1:c.3272G>A	NP_001124449.1:p.Gly1091Glu
NM_001130977.2:c.3272G>A	NP_001124449.1:p.Gly1091Glu
NM_001130978.1:c.3314G>A	NP_001124450.1:p.Gly1105Glu
NM_001130978.2:c.3314G>A	NP_001124450.1:p.Gly1105Glu
NM_001130979.1:c.3407G>A	NP_001124451.1:p.Gly1136Glu
NM_001130979.2:c.3407G>A	NP_001124451.1:p.Gly1136Glu
NM_001130980.1:c.3365G>A	NP_001124452.1:p.Gly1122Glu
NM_001130980.2:c.3365G>A	NP_001124452.1:p.Gly1122Glu
NM_001130981.1:c.3365G>A	NP_001124453.1:p.Gly1122Glu
NM_001130981.2:c.3365G>A	NP_001124453.1:p.Gly1122Glu
NM_001130982.1:c.3410G>A	NP_001124454.1:p.Gly1137Glu
NM_001130982.2:c.3410G>A	NP_001124454.1:p.Gly1137Glu
NM_001130983.1:c.3317G>A	NP_001124455.1:p.Gly1106Glu
NM_001130983.2:c.3317G>A	NP_001124455.1:p.Gly1106Glu
NM_001130984.1:c.3275G>A	NP_001124456.1:p.Gly1092Glu
NM_001130984.2:c.3275G>A	NP_001124456.1:p.Gly1092Glu
NM_001130985.1:c.3368G>A	NP_001124457.1:p.Gly1123Glu
NM_001130985.2:c.3368G>A	NP_001124457.1:p.Gly1123Glu
NM_001130986.1:c.3275G>A	NP_001124458.1:p.Gly1092Glu
NM_001130986.2:c.3275G>A	NP_001124458.1:p.Gly1092Glu
NM_001130987.1:c.3368G>A	NP_001124459.1:p.Gly1123Glu
NM_003494.3:c.3314G>A	NP_003485.1:p.Gly1105Glu
ENST00000258104.7:c.3314G>A	ENSP00000258104.3:p.Gly1105Glu
ENST00000394120.6:c.3317G>A	ENSP00000377678.2:p.Gly1106Glu
ENST00000409366.5:c.3317G>A	ENSP00000386512.1:p.Gly1106Glu
ENST00000409582.7:c.3365G>A	ENSP00000386547.3:p.Gly1122Glu
ENST00000409651.5:c.3410G>A	ENSP00000386683.1:p.Gly1137Glu
ENST00000409744.5:c.3275G>A	ENSP00000386285.1:p.Gly1092Glu
ENST00000409762.5:c.3365G>A	ENSP00000387137.1:p.Gly1122Glu
ENST00000410020.7:c.3368G>A	ENSP00000386881.3:p.Gly1123Glu
ENST00000410041.1:c.3368G>A	ENSP00000386617.1:p.Gly1123Glu
ENST00000413539.6:c.3407G>A	ENSP00000407046.2:p.Gly1136Glu
ENST00000429174.6:c.3314G>A	ENSP00000398305.2:p.Gly1105Glu
ENST00000698057.1:c.740G>A	ENSP00000513536.1:p.Gly247Glu
XM_005264584.3:c.3410G>A	XP_005264641.1:p.Gly1137Glu
XM_005264584.4:c.3410G>A	XP_005264641.1:p.Gly1137Glu
XM_005264585.3:c.3407G>A	XP_005264642.1:p.Gly1136Glu
XM_005264585.5:c.3407G>A	XP_005264642.1:p.Gly1136Glu
XR_001738969.1:n.3568G>A