Canonical Allele Identifier: CA347224087

Gene: DYSF

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.3176A>C	ENSP00000513536.1:p.Gln1059Pro
ENST00000698058.1:c.2393A>C	ENSP00000513537.1:p.Gln798Pro
ENST00000698059.1:c.2501A>C	ENSP00000513538.1:p.Gln834Pro
ENST00000258104.8:c.5645A>C MANE Plus Clinical	ENSP00000258104.3:p.Gln1882Pro
ENST00000410020.8:c.5762A>C MANE Select	ENSP00000386881.3:p.Gln1921Pro
ENST00000258104.7:c.5645A>C	ENSP00000258104.3:p.Gln1882Pro
ENST00000394120.6:c.5648A>C	ENSP00000377678.2:p.Gln1883Pro
ENST00000409366.5:c.5711A>C	ENSP00000386512.1:p.Gln1904Pro
ENST00000409582.7:c.5759A>C	ENSP00000386547.3:p.Gln1920Pro
ENST00000409651.5:c.5741A>C	ENSP00000386683.1:p.Gln1914Pro
ENST00000409744.5:c.5669A>C	ENSP00000386285.1:p.Gln1890Pro
ENST00000409762.5:c.5696A>C	ENSP00000387137.1:p.Gln1899Pro
ENST00000410020.7:c.5762A>C	ENSP00000386881.3:p.Gln1921Pro
ENST00000410041.1:c.5699A>C	ENSP00000386617.1:p.Gln1900Pro
ENST00000413539.6:c.5738A>C	ENSP00000407046.2:p.Gln1913Pro
ENST00000429174.6:c.5708A>C	ENSP00000398305.2:p.Gln1903Pro
ENST00000479049.6:n.2530A>C
NM_001130455.1:c.5648A>C	NP_001123927.1:p.Gln1883Pro
NM_001130976.1:c.5603A>C	NP_001124448.1:p.Gln1868Pro
NM_001130977.1:c.5666A>C	NP_001124449.1:p.Gln1889Pro
NM_001130978.1:c.5708A>C	NP_001124450.1:p.Gln1903Pro
NM_001130979.1:c.5738A>C	NP_001124451.1:p.Gln1913Pro
NM_001130980.1:c.5696A>C	NP_001124452.1:p.Gln1899Pro
NM_001130981.1:c.5759A>C	NP_001124453.1:p.Gln1920Pro
NM_001130982.1:c.5741A>C	NP_001124454.1:p.Gln1914Pro
NM_001130983.1:c.5711A>C	NP_001124455.1:p.Gln1904Pro
NM_001130984.1:c.5669A>C	NP_001124456.1:p.Gln1890Pro
NM_001130985.1:c.5699A>C	NP_001124457.1:p.Gln1900Pro
NM_001130986.1:c.5606A>C	NP_001124458.1:p.Gln1869Pro
NM_001130987.1:c.5762A>C	NP_001124459.1:p.Gln1921Pro
NM_003494.3:c.5645A>C	NP_003485.1:p.Gln1882Pro
XM_005264584.3:c.5804A>C	XP_005264641.1:p.Gln1935Pro
XM_005264585.3:c.5801A>C	XP_005264642.1:p.Gln1934Pro
XM_005264584.4:c.5804A>C	XP_005264641.1:p.Gln1935Pro
XM_005264585.5:c.5801A>C	XP_005264642.1:p.Gln1934Pro
NM_001130987.2:c.5762A>C MANE Select	NP_001124459.1:p.Gln1921Pro
NM_001130455.2:c.5648A>C	NP_001123927.1:p.Gln1883Pro
NM_001130976.2:c.5603A>C	NP_001124448.1:p.Gln1868Pro
NM_001130977.2:c.5666A>C	NP_001124449.1:p.Gln1889Pro
NM_001130978.2:c.5708A>C	NP_001124450.1:p.Gln1903Pro
NM_001130979.2:c.5738A>C	NP_001124451.1:p.Gln1913Pro
NM_001130980.2:c.5696A>C	NP_001124452.1:p.Gln1899Pro
NM_001130981.2:c.5759A>C	NP_001124453.1:p.Gln1920Pro
NM_001130982.2:c.5741A>C	NP_001124454.1:p.Gln1914Pro
NM_001130983.2:c.5711A>C	NP_001124455.1:p.Gln1904Pro
NM_001130984.2:c.5669A>C	NP_001124456.1:p.Gln1890Pro
NM_001130985.2:c.5699A>C	NP_001124457.1:p.Gln1900Pro
NM_001130986.2:c.5606A>C	NP_001124458.1:p.Gln1869Pro
NM_003494.4:c.5645A>C MANE Plus Clinical	NP_003485.1:p.Gln1882Pro