Canonical Allele Identifier: CA347219585

Gene: DYSF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71658877G>A , CM000664.2:g.71658877G>A	GRCh38
NC_000002.11:g.71886007G>A , CM000664.1:g.71886007G>A	GRCh37
NC_000002.10:g.71739515G>A	NCBI36
NG_008694.1:g.210255G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001130987.2:c.4756-1G>A MANE Select	NP_001124459.1:n.4756-1G>A
ENST00000410020.8:c.4756-1G>A MANE Select	ENSP00000386881.3:n.4756-1G>A
NM_003494.4:c.4639-1G>A MANE Plus Clinical	NP_003485.1:n.4639-1G>A
ENST00000258104.8:c.4639-1G>A MANE Plus Clinical	ENSP00000258104.3:n.4639-1G>A
NM_001130455.1:c.4642-1G>A	NP_001123927.1:n.4642-1G>A
NM_001130455.2:c.4642-1G>A	NP_001123927.1:n.4642-1G>A
NM_001130976.1:c.4597-1G>A	NP_001124448.1:n.4597-1G>A
NM_001130976.2:c.4597-1G>A	NP_001124448.1:n.4597-1G>A
NM_001130977.1:c.4660-1G>A	NP_001124449.1:n.4660-1G>A
NM_001130977.2:c.4660-1G>A	NP_001124449.1:n.4660-1G>A
NM_001130978.1:c.4702-1G>A	NP_001124450.1:n.4702-1G>A
NM_001130978.2:c.4702-1G>A	NP_001124450.1:n.4702-1G>A
NM_001130979.1:c.4732-1G>A	NP_001124451.1:n.4732-1G>A
NM_001130979.2:c.4732-1G>A	NP_001124451.1:n.4732-1G>A
NM_001130980.1:c.4690-1G>A	NP_001124452.1:n.4690-1G>A
NM_001130980.2:c.4690-1G>A	NP_001124452.1:n.4690-1G>A
NM_001130981.1:c.4753-1G>A	NP_001124453.1:n.4753-1G>A
NM_001130981.2:c.4753-1G>A	NP_001124453.1:n.4753-1G>A
NM_001130982.1:c.4735-1G>A	NP_001124454.1:n.4735-1G>A
NM_001130982.2:c.4735-1G>A	NP_001124454.1:n.4735-1G>A
NM_001130983.1:c.4705-1G>A	NP_001124455.1:n.4705-1G>A
NM_001130983.2:c.4705-1G>A	NP_001124455.1:n.4705-1G>A
NM_001130984.1:c.4663-1G>A	NP_001124456.1:n.4663-1G>A
NM_001130984.2:c.4663-1G>A	NP_001124456.1:n.4663-1G>A
NM_001130985.1:c.4693-1G>A	NP_001124457.1:n.4693-1G>A
NM_001130985.2:c.4693-1G>A	NP_001124457.1:n.4693-1G>A
NM_001130986.1:c.4600-1G>A	NP_001124458.1:n.4600-1G>A
NM_001130986.2:c.4600-1G>A	NP_001124458.1:n.4600-1G>A
NM_001130987.1:c.4756-1G>A	NP_001124459.1:n.4756-1G>A
NM_003494.3:c.4639-1G>A	NP_003485.1:n.4639-1G>A
ENST00000258104.7:c.4639-1G>A	ENSP00000258104.3:n.4639-1G>A
ENST00000394120.6:c.4642-1G>A	ENSP00000377678.2:n.4642-1G>A
ENST00000409366.5:c.4705-1G>A	ENSP00000386512.1:n.4705-1G>A
ENST00000409582.7:c.4753-1G>A	ENSP00000386547.3:n.4753-1G>A
ENST00000409651.5:c.4735-1G>A	ENSP00000386683.1:n.4735-1G>A
ENST00000409744.5:c.4663-1G>A	ENSP00000386285.1:n.4663-1G>A
ENST00000409762.5:c.4690-1G>A	ENSP00000387137.1:n.4690-1G>A
ENST00000410020.7:c.4756-1G>A	ENSP00000386881.3:n.4756-1G>A
ENST00000410041.1:c.4693-1G>A	ENSP00000386617.1:n.4693-1G>A
ENST00000413539.6:c.4732-1G>A	ENSP00000407046.2:n.4732-1G>A
ENST00000429174.6:c.4702-1G>A	ENSP00000398305.2:n.4702-1G>A
ENST00000479049.6:n.1524-1G>A
ENST00000698057.1:c.2170-1G>A	ENSP00000513536.1:n.2170-1G>A
ENST00000698058.1:c.1387-1G>A	ENSP00000513537.1:n.1387-1G>A
ENST00000698059.1:c.1495-1G>A	ENSP00000513538.1:n.1495-1G>A
XM_005264584.3:c.4798-1G>A	XP_005264641.1:n.4798-1G>A
XM_005264584.4:c.4798-1G>A	XP_005264641.1:n.4798-1G>A
XM_005264585.3:c.4795-1G>A	XP_005264642.1:n.4795-1G>A
XM_005264585.5:c.4795-1G>A	XP_005264642.1:n.4795-1G>A
XR_001738969.1:n.4956-1G>A