Canonical Allele Identifier: CA1260124129

Gene: DYSF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71611481T= , CM000664.2:g.71611481T=	GRCh38
NC_000002.11:g.71838611T= , CM000664.1:g.71838611T=	GRCh37
NC_000002.10:g.71692119T=	NCBI36
NG_008694.1:g.162859T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.1490T=	ENSP00000513536.1:p.Leu497=
ENST00000698058.1:c.707T=	ENSP00000513537.1:p.Leu236=
ENST00000698059.1:c.665T=	ENSP00000513538.1:p.Leu222=
ENST00000258104.8:c.4022T= MANE Plus Clinical	ENSP00000258104.3:p.Leu1341=
ENST00000410020.8:c.4076T= MANE Select	ENSP00000386881.3:p.Leu1359=
ENST00000258104.7:c.4022T=	ENSP00000258104.3:p.Leu1341=
ENST00000394120.6:c.4025T=	ENSP00000377678.2:p.Leu1342=
ENST00000409366.5:c.4025T=	ENSP00000386512.1:p.Leu1342=
ENST00000409582.7:c.4073T=	ENSP00000386547.3:p.Leu1358=
ENST00000409651.5:c.4118T=	ENSP00000386683.1:p.Leu1373=
ENST00000409744.5:c.3983T=	ENSP00000386285.1:p.Leu1328=
ENST00000409762.5:c.4073T=	ENSP00000387137.1:p.Leu1358=
ENST00000410020.7:c.4076T=	ENSP00000386881.3:p.Leu1359=
ENST00000410041.1:c.4076T=	ENSP00000386617.1:p.Leu1359=
ENST00000413539.6:c.4115T=	ENSP00000407046.2:p.Leu1372=
ENST00000429174.6:c.4022T=	ENSP00000398305.2:p.Leu1341=
ENST00000468173.1:n.258T=
ENST00000472873.5:n.406T=
ENST00000479049.6:n.907T=
ENST00000487180.5:n.241T=
ENST00000494501.5:n.366-46T=
NM_001130455.1:c.4025T=	NP_001123927.1:p.Leu1342=
NM_001130976.1:c.3980T=	NP_001124448.1:p.Leu1327=
NM_001130977.1:c.3980T=	NP_001124449.1:p.Leu1327=
NM_001130978.1:c.4022T=	NP_001124450.1:p.Leu1341=
NM_001130979.1:c.4115T=	NP_001124451.1:p.Leu1372=
NM_001130980.1:c.4073T=	NP_001124452.1:p.Leu1358=
NM_001130981.1:c.4073T=	NP_001124453.1:p.Leu1358=
NM_001130982.1:c.4118T=	NP_001124454.1:p.Leu1373=
NM_001130983.1:c.4025T=	NP_001124455.1:p.Leu1342=
NM_001130984.1:c.3983T=	NP_001124456.1:p.Leu1328=
NM_001130985.1:c.4076T=	NP_001124457.1:p.Leu1359=
NM_001130986.1:c.3983T=	NP_001124458.1:p.Leu1328=
NM_001130987.1:c.4076T=	NP_001124459.1:p.Leu1359=
NM_003494.3:c.4022T=	NP_003485.1:p.Leu1341=
XM_005264584.3:c.4118T=	XP_005264641.1:p.Leu1373=
XM_005264585.3:c.4115T=	XP_005264642.1:p.Leu1372=
XM_005264584.4:c.4118T=	XP_005264641.1:p.Leu1373=
XM_005264585.5:c.4115T=	XP_005264642.1:p.Leu1372=
XR_001738969.1:n.4276T=
NM_001130987.2:c.4076T= MANE Select	NP_001124459.1:p.Leu1359=
NM_001130455.2:c.4025T=	NP_001123927.1:p.Leu1342=
NM_001130976.2:c.3980T=	NP_001124448.1:p.Leu1327=
NM_001130977.2:c.3980T=	NP_001124449.1:p.Leu1327=
NM_001130978.2:c.4022T=	NP_001124450.1:p.Leu1341=
NM_001130979.2:c.4115T=	NP_001124451.1:p.Leu1372=
NM_001130980.2:c.4073T=	NP_001124452.1:p.Leu1358=
NM_001130981.2:c.4073T=	NP_001124453.1:p.Leu1358=
NM_001130982.2:c.4118T=	NP_001124454.1:p.Leu1373=
NM_001130983.2:c.4025T=	NP_001124455.1:p.Leu1342=
NM_001130984.2:c.3983T=	NP_001124456.1:p.Leu1328=
NM_001130985.2:c.4076T=	NP_001124457.1:p.Leu1359=
NM_001130986.2:c.3983T=	NP_001124458.1:p.Leu1328=
NM_003494.4:c.4022T= MANE Plus Clinical	NP_003485.1:p.Leu1341=