Canonical Allele Identifier: CA1260124164

Gene: DYSF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71611554G= , CM000664.2:g.71611554G=	GRCh38
NC_000002.11:g.71838684G= , CM000664.1:g.71838684G=	GRCh37
NC_000002.10:g.71692192G=	NCBI36
NG_008694.1:g.162932G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.1563G=	ENSP00000513536.1:p.Thr521=
ENST00000698058.1:c.780G=	ENSP00000513537.1:p.Thr260=
ENST00000698059.1:c.738G=	ENSP00000513538.1:p.Thr246=
ENST00000258104.8:c.4095G= MANE Plus Clinical	ENSP00000258104.3:p.Thr1365=
ENST00000410020.8:c.4149G= MANE Select	ENSP00000386881.3:p.Thr1383=
ENST00000258104.7:c.4095G=	ENSP00000258104.3:p.Thr1365=
ENST00000394120.6:c.4098G=	ENSP00000377678.2:p.Thr1366=
ENST00000409366.5:c.4098G=	ENSP00000386512.1:p.Thr1366=
ENST00000409582.7:c.4146G=	ENSP00000386547.3:p.Thr1382=
ENST00000409651.5:c.4191G=	ENSP00000386683.1:p.Thr1397=
ENST00000409744.5:c.4056G=	ENSP00000386285.1:p.Thr1352=
ENST00000409762.5:c.4146G=	ENSP00000387137.1:p.Thr1382=
ENST00000410020.7:c.4149G=	ENSP00000386881.3:p.Thr1383=
ENST00000410041.1:c.4149G=	ENSP00000386617.1:p.Thr1383=
ENST00000413539.6:c.4188G=	ENSP00000407046.2:p.Thr1396=
ENST00000429174.6:c.4095G=	ENSP00000398305.2:p.Thr1365=
ENST00000468173.1:n.331G=
ENST00000472873.5:n.479G=
ENST00000479049.6:n.980G=
ENST00000487180.5:n.314G=
ENST00000494501.5:n.393G=
NM_001130455.1:c.4098G=	NP_001123927.1:p.Thr1366=
NM_001130976.1:c.4053G=	NP_001124448.1:p.Thr1351=
NM_001130977.1:c.4053G=	NP_001124449.1:p.Thr1351=
NM_001130978.1:c.4095G=	NP_001124450.1:p.Thr1365=
NM_001130979.1:c.4188G=	NP_001124451.1:p.Thr1396=
NM_001130980.1:c.4146G=	NP_001124452.1:p.Thr1382=
NM_001130981.1:c.4146G=	NP_001124453.1:p.Thr1382=
NM_001130982.1:c.4191G=	NP_001124454.1:p.Thr1397=
NM_001130983.1:c.4098G=	NP_001124455.1:p.Thr1366=
NM_001130984.1:c.4056G=	NP_001124456.1:p.Thr1352=
NM_001130985.1:c.4149G=	NP_001124457.1:p.Thr1383=
NM_001130986.1:c.4056G=	NP_001124458.1:p.Thr1352=
NM_001130987.1:c.4149G=	NP_001124459.1:p.Thr1383=
NM_003494.3:c.4095G=	NP_003485.1:p.Thr1365=
XM_005264584.3:c.4191G=	XP_005264641.1:p.Thr1397=
XM_005264585.3:c.4188G=	XP_005264642.1:p.Thr1396=
XM_005264584.4:c.4191G=	XP_005264641.1:p.Thr1397=
XM_005264585.5:c.4188G=	XP_005264642.1:p.Thr1396=
XR_001738969.1:n.4349G=
NM_001130987.2:c.4149G= MANE Select	NP_001124459.1:p.Thr1383=
NM_001130455.2:c.4098G=	NP_001123927.1:p.Thr1366=
NM_001130976.2:c.4053G=	NP_001124448.1:p.Thr1351=
NM_001130977.2:c.4053G=	NP_001124449.1:p.Thr1351=
NM_001130978.2:c.4095G=	NP_001124450.1:p.Thr1365=
NM_001130979.2:c.4188G=	NP_001124451.1:p.Thr1396=
NM_001130980.2:c.4146G=	NP_001124452.1:p.Thr1382=
NM_001130981.2:c.4146G=	NP_001124453.1:p.Thr1382=
NM_001130982.2:c.4191G=	NP_001124454.1:p.Thr1397=
NM_001130983.2:c.4098G=	NP_001124455.1:p.Thr1366=
NM_001130984.2:c.4056G=	NP_001124456.1:p.Thr1352=
NM_001130985.2:c.4149G=	NP_001124457.1:p.Thr1383=
NM_001130986.2:c.4056G=	NP_001124458.1:p.Thr1352=
NM_003494.4:c.4095G= MANE Plus Clinical	NP_003485.1:p.Thr1365=