Canonical Allele Identifier: CA347217874

Gene: DYSF

Linked Data

• MyVariant Identifiers: chr2:g.71871125T>A (hg19) ; chr2:g.71643995T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71643995T>A , CM000664.2:g.71643995T>A	GRCh38
NC_000002.11:g.71871125T>A , CM000664.1:g.71871125T>A	GRCh37
NC_000002.10:g.71724633T>A	NCBI36
NG_008694.1:g.195373T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.1972T>A	ENSP00000513536.1:p.Phe658Ile
ENST00000698058.1:c.1189T>A	ENSP00000513537.1:p.Phe397Ile
ENST00000698059.1:c.1297T>A	ENSP00000513538.1:p.Phe433Ile
ENST00000258104.8:c.4441T>A MANE Plus Clinical	ENSP00000258104.3:p.Phe1481Ile
ENST00000410020.8:c.4558T>A MANE Select	ENSP00000386881.3:p.Phe1520Ile
ENST00000258104.7:c.4441T>A	ENSP00000258104.3:p.Phe1481Ile
ENST00000394120.6:c.4444T>A	ENSP00000377678.2:p.Phe1482Ile
ENST00000409366.5:c.4507T>A	ENSP00000386512.1:p.Phe1503Ile
ENST00000409582.7:c.4555T>A	ENSP00000386547.3:p.Phe1519Ile
ENST00000409651.5:c.4537T>A	ENSP00000386683.1:p.Phe1513Ile
ENST00000409744.5:c.4465T>A	ENSP00000386285.1:p.Phe1489Ile
ENST00000409762.5:c.4492T>A	ENSP00000387137.1:p.Phe1498Ile
ENST00000410020.7:c.4558T>A	ENSP00000386881.3:p.Phe1520Ile
ENST00000410041.1:c.4495T>A	ENSP00000386617.1:p.Phe1499Ile
ENST00000413539.6:c.4534T>A	ENSP00000407046.2:p.Phe1512Ile
ENST00000429174.6:c.4504T>A	ENSP00000398305.2:p.Phe1502Ile
ENST00000468173.1:n.740T>A
ENST00000479049.6:n.1326T>A
NM_001130455.1:c.4444T>A	NP_001123927.1:p.Phe1482Ile
NM_001130976.1:c.4399T>A	NP_001124448.1:p.Phe1467Ile
NM_001130977.1:c.4462T>A	NP_001124449.1:p.Phe1488Ile
NM_001130978.1:c.4504T>A	NP_001124450.1:p.Phe1502Ile
NM_001130979.1:c.4534T>A	NP_001124451.1:p.Phe1512Ile
NM_001130980.1:c.4492T>A	NP_001124452.1:p.Phe1498Ile
NM_001130981.1:c.4555T>A	NP_001124453.1:p.Phe1519Ile
NM_001130982.1:c.4537T>A	NP_001124454.1:p.Phe1513Ile
NM_001130983.1:c.4507T>A	NP_001124455.1:p.Phe1503Ile
NM_001130984.1:c.4465T>A	NP_001124456.1:p.Phe1489Ile
NM_001130985.1:c.4495T>A	NP_001124457.1:p.Phe1499Ile
NM_001130986.1:c.4402T>A	NP_001124458.1:p.Phe1468Ile
NM_001130987.1:c.4558T>A	NP_001124459.1:p.Phe1520Ile
NM_003494.3:c.4441T>A	NP_003485.1:p.Phe1481Ile
XM_005264584.3:c.4600T>A	XP_005264641.1:p.Phe1534Ile
XM_005264585.3:c.4597T>A	XP_005264642.1:p.Phe1533Ile
XM_005264584.4:c.4600T>A	XP_005264641.1:p.Phe1534Ile
XM_005264585.5:c.4597T>A	XP_005264642.1:p.Phe1533Ile
XR_001738969.1:n.4758T>A
NM_001130987.2:c.4558T>A MANE Select	NP_001124459.1:p.Phe1520Ile
NM_001130455.2:c.4444T>A	NP_001123927.1:p.Phe1482Ile
NM_001130976.2:c.4399T>A	NP_001124448.1:p.Phe1467Ile
NM_001130977.2:c.4462T>A	NP_001124449.1:p.Phe1488Ile
NM_001130978.2:c.4504T>A	NP_001124450.1:p.Phe1502Ile
NM_001130979.2:c.4534T>A	NP_001124451.1:p.Phe1512Ile
NM_001130980.2:c.4492T>A	NP_001124452.1:p.Phe1498Ile
NM_001130981.2:c.4555T>A	NP_001124453.1:p.Phe1519Ile
NM_001130982.2:c.4537T>A	NP_001124454.1:p.Phe1513Ile
NM_001130983.2:c.4507T>A	NP_001124455.1:p.Phe1503Ile
NM_001130984.2:c.4465T>A	NP_001124456.1:p.Phe1489Ile
NM_001130985.2:c.4495T>A	NP_001124457.1:p.Phe1499Ile
NM_001130986.2:c.4402T>A	NP_001124458.1:p.Phe1468Ile
NM_003494.4:c.4441T>A MANE Plus Clinical	NP_003485.1:p.Phe1481Ile