Canonical Allele Identifier: CA347224090

Gene: DYSF

Linked Data

• MyVariant Identifiers: chr2:g.71896854A>G (hg19) ; chr2:g.71669724A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71669724A>G , CM000664.2:g.71669724A>G	GRCh38
NC_000002.11:g.71896854A>G , CM000664.1:g.71896854A>G	GRCh37
NC_000002.10:g.71750362A>G	NCBI36
NG_008694.1:g.221102A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.3176A>G	ENSP00000513536.1:p.Gln1059Arg
ENST00000698058.1:c.2393A>G	ENSP00000513537.1:p.Gln798Arg
ENST00000698059.1:c.2501A>G	ENSP00000513538.1:p.Gln834Arg
ENST00000258104.8:c.5645A>G MANE Plus Clinical	ENSP00000258104.3:p.Gln1882Arg
ENST00000410020.8:c.5762A>G MANE Select	ENSP00000386881.3:p.Gln1921Arg
ENST00000258104.7:c.5645A>G	ENSP00000258104.3:p.Gln1882Arg
ENST00000394120.6:c.5648A>G	ENSP00000377678.2:p.Gln1883Arg
ENST00000409366.5:c.5711A>G	ENSP00000386512.1:p.Gln1904Arg
ENST00000409582.7:c.5759A>G	ENSP00000386547.3:p.Gln1920Arg
ENST00000409651.5:c.5741A>G	ENSP00000386683.1:p.Gln1914Arg
ENST00000409744.5:c.5669A>G	ENSP00000386285.1:p.Gln1890Arg
ENST00000409762.5:c.5696A>G	ENSP00000387137.1:p.Gln1899Arg
ENST00000410020.7:c.5762A>G	ENSP00000386881.3:p.Gln1921Arg
ENST00000410041.1:c.5699A>G	ENSP00000386617.1:p.Gln1900Arg
ENST00000413539.6:c.5738A>G	ENSP00000407046.2:p.Gln1913Arg
ENST00000429174.6:c.5708A>G	ENSP00000398305.2:p.Gln1903Arg
ENST00000479049.6:n.2530A>G
NM_001130455.1:c.5648A>G	NP_001123927.1:p.Gln1883Arg
NM_001130976.1:c.5603A>G	NP_001124448.1:p.Gln1868Arg
NM_001130977.1:c.5666A>G	NP_001124449.1:p.Gln1889Arg
NM_001130978.1:c.5708A>G	NP_001124450.1:p.Gln1903Arg
NM_001130979.1:c.5738A>G	NP_001124451.1:p.Gln1913Arg
NM_001130980.1:c.5696A>G	NP_001124452.1:p.Gln1899Arg
NM_001130981.1:c.5759A>G	NP_001124453.1:p.Gln1920Arg
NM_001130982.1:c.5741A>G	NP_001124454.1:p.Gln1914Arg
NM_001130983.1:c.5711A>G	NP_001124455.1:p.Gln1904Arg
NM_001130984.1:c.5669A>G	NP_001124456.1:p.Gln1890Arg
NM_001130985.1:c.5699A>G	NP_001124457.1:p.Gln1900Arg
NM_001130986.1:c.5606A>G	NP_001124458.1:p.Gln1869Arg
NM_001130987.1:c.5762A>G	NP_001124459.1:p.Gln1921Arg
NM_003494.3:c.5645A>G	NP_003485.1:p.Gln1882Arg
XM_005264584.3:c.5804A>G	XP_005264641.1:p.Gln1935Arg
XM_005264585.3:c.5801A>G	XP_005264642.1:p.Gln1934Arg
XM_005264584.4:c.5804A>G	XP_005264641.1:p.Gln1935Arg
XM_005264585.5:c.5801A>G	XP_005264642.1:p.Gln1934Arg
NM_001130987.2:c.5762A>G MANE Select	NP_001124459.1:p.Gln1921Arg
NM_001130455.2:c.5648A>G	NP_001123927.1:p.Gln1883Arg
NM_001130976.2:c.5603A>G	NP_001124448.1:p.Gln1868Arg
NM_001130977.2:c.5666A>G	NP_001124449.1:p.Gln1889Arg
NM_001130978.2:c.5708A>G	NP_001124450.1:p.Gln1903Arg
NM_001130979.2:c.5738A>G	NP_001124451.1:p.Gln1913Arg
NM_001130980.2:c.5696A>G	NP_001124452.1:p.Gln1899Arg
NM_001130981.2:c.5759A>G	NP_001124453.1:p.Gln1920Arg
NM_001130982.2:c.5741A>G	NP_001124454.1:p.Gln1914Arg
NM_001130983.2:c.5711A>G	NP_001124455.1:p.Gln1904Arg
NM_001130984.2:c.5669A>G	NP_001124456.1:p.Gln1890Arg
NM_001130985.2:c.5699A>G	NP_001124457.1:p.Gln1900Arg
NM_001130986.2:c.5606A>G	NP_001124458.1:p.Gln1869Arg
NM_003494.4:c.5645A>G MANE Plus Clinical	NP_003485.1:p.Gln1882Arg