Canonical Allele Identifier: CA1260124148

Gene: DYSF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71611524C= , CM000664.2:g.71611524C=	GRCh38
NC_000002.11:g.71838654C= , CM000664.1:g.71838654C=	GRCh37
NC_000002.10:g.71692162C=	NCBI36
NG_008694.1:g.162902C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.1533C=	ENSP00000513536.1:p.Pro511=
ENST00000698058.1:c.750C=	ENSP00000513537.1:p.Pro250=
ENST00000698059.1:c.708C=	ENSP00000513538.1:p.Pro236=
ENST00000258104.8:c.4065C= MANE Plus Clinical	ENSP00000258104.3:p.Pro1355=
ENST00000410020.8:c.4119C= MANE Select	ENSP00000386881.3:p.Pro1373=
ENST00000258104.7:c.4065C=	ENSP00000258104.3:p.Pro1355=
ENST00000394120.6:c.4068C=	ENSP00000377678.2:p.Pro1356=
ENST00000409366.5:c.4068C=	ENSP00000386512.1:p.Pro1356=
ENST00000409582.7:c.4116C=	ENSP00000386547.3:p.Pro1372=
ENST00000409651.5:c.4161C=	ENSP00000386683.1:p.Pro1387=
ENST00000409744.5:c.4026C=	ENSP00000386285.1:p.Pro1342=
ENST00000409762.5:c.4116C=	ENSP00000387137.1:p.Pro1372=
ENST00000410020.7:c.4119C=	ENSP00000386881.3:p.Pro1373=
ENST00000410041.1:c.4119C=	ENSP00000386617.1:p.Pro1373=
ENST00000413539.6:c.4158C=	ENSP00000407046.2:p.Pro1386=
ENST00000429174.6:c.4065C=	ENSP00000398305.2:p.Pro1355=
ENST00000468173.1:n.301C=
ENST00000472873.5:n.449C=
ENST00000479049.6:n.950C=
ENST00000487180.5:n.284C=
ENST00000494501.5:n.366-3C=
NM_001130455.1:c.4068C=	NP_001123927.1:p.Pro1356=
NM_001130976.1:c.4023C=	NP_001124448.1:p.Pro1341=
NM_001130977.1:c.4023C=	NP_001124449.1:p.Pro1341=
NM_001130978.1:c.4065C=	NP_001124450.1:p.Pro1355=
NM_001130979.1:c.4158C=	NP_001124451.1:p.Pro1386=
NM_001130980.1:c.4116C=	NP_001124452.1:p.Pro1372=
NM_001130981.1:c.4116C=	NP_001124453.1:p.Pro1372=
NM_001130982.1:c.4161C=	NP_001124454.1:p.Pro1387=
NM_001130983.1:c.4068C=	NP_001124455.1:p.Pro1356=
NM_001130984.1:c.4026C=	NP_001124456.1:p.Pro1342=
NM_001130985.1:c.4119C=	NP_001124457.1:p.Pro1373=
NM_001130986.1:c.4026C=	NP_001124458.1:p.Pro1342=
NM_001130987.1:c.4119C=	NP_001124459.1:p.Pro1373=
NM_003494.3:c.4065C=	NP_003485.1:p.Pro1355=
XM_005264584.3:c.4161C=	XP_005264641.1:p.Pro1387=
XM_005264585.3:c.4158C=	XP_005264642.1:p.Pro1386=
XM_005264584.4:c.4161C=	XP_005264641.1:p.Pro1387=
XM_005264585.5:c.4158C=	XP_005264642.1:p.Pro1386=
XR_001738969.1:n.4319C=
NM_001130987.2:c.4119C= MANE Select	NP_001124459.1:p.Pro1373=
NM_001130455.2:c.4068C=	NP_001123927.1:p.Pro1356=
NM_001130976.2:c.4023C=	NP_001124448.1:p.Pro1341=
NM_001130977.2:c.4023C=	NP_001124449.1:p.Pro1341=
NM_001130978.2:c.4065C=	NP_001124450.1:p.Pro1355=
NM_001130979.2:c.4158C=	NP_001124451.1:p.Pro1386=
NM_001130980.2:c.4116C=	NP_001124452.1:p.Pro1372=
NM_001130981.2:c.4116C=	NP_001124453.1:p.Pro1372=
NM_001130982.2:c.4161C=	NP_001124454.1:p.Pro1387=
NM_001130983.2:c.4068C=	NP_001124455.1:p.Pro1356=
NM_001130984.2:c.4026C=	NP_001124456.1:p.Pro1342=
NM_001130985.2:c.4119C=	NP_001124457.1:p.Pro1373=
NM_001130986.2:c.4026C=	NP_001124458.1:p.Pro1342=
NM_003494.4:c.4065C= MANE Plus Clinical	NP_003485.1:p.Pro1355=