Canonical Allele Identifier: CA347223079

Gene: DYSF

Linked Data

• MyVariant Identifiers: chr2:g.71896321G>T (hg19) ; chr2:g.71669191G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71669191G>T , CM000664.2:g.71669191G>T	GRCh38
NC_000002.11:g.71896321G>T , CM000664.1:g.71896321G>T	GRCh37
NC_000002.10:g.71749829G>T	NCBI36
NG_008694.1:g.220569G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.3040G>T	ENSP00000513536.1:p.Asp1014Tyr
ENST00000698058.1:c.2257G>T	ENSP00000513537.1:p.Asp753Tyr
ENST00000698059.1:c.2365G>T	ENSP00000513538.1:p.Asp789Tyr
ENST00000258104.8:c.5509G>T MANE Plus Clinical	ENSP00000258104.3:p.Asp1837Tyr
ENST00000410020.8:c.5626G>T MANE Select	ENSP00000386881.3:p.Asp1876Tyr
ENST00000258104.7:c.5509G>T	ENSP00000258104.3:p.Asp1837Tyr
ENST00000394120.6:c.5512G>T	ENSP00000377678.2:p.Asp1838Tyr
ENST00000409366.5:c.5575G>T	ENSP00000386512.1:p.Asp1859Tyr
ENST00000409582.7:c.5623G>T	ENSP00000386547.3:p.Asp1875Tyr
ENST00000409651.5:c.5605G>T	ENSP00000386683.1:p.Asp1869Tyr
ENST00000409744.5:c.5533G>T	ENSP00000386285.1:p.Asp1845Tyr
ENST00000409762.5:c.5560G>T	ENSP00000387137.1:p.Asp1854Tyr
ENST00000410020.7:c.5626G>T	ENSP00000386881.3:p.Asp1876Tyr
ENST00000410041.1:c.5563G>T	ENSP00000386617.1:p.Asp1855Tyr
ENST00000413539.6:c.5602G>T	ENSP00000407046.2:p.Asp1868Tyr
ENST00000429174.6:c.5572G>T	ENSP00000398305.2:p.Asp1858Tyr
ENST00000479049.6:n.2394G>T
NM_001130455.1:c.5512G>T	NP_001123927.1:p.Asp1838Tyr
NM_001130976.1:c.5467G>T	NP_001124448.1:p.Asp1823Tyr
NM_001130977.1:c.5530G>T	NP_001124449.1:p.Asp1844Tyr
NM_001130978.1:c.5572G>T	NP_001124450.1:p.Asp1858Tyr
NM_001130979.1:c.5602G>T	NP_001124451.1:p.Asp1868Tyr
NM_001130980.1:c.5560G>T	NP_001124452.1:p.Asp1854Tyr
NM_001130981.1:c.5623G>T	NP_001124453.1:p.Asp1875Tyr
NM_001130982.1:c.5605G>T	NP_001124454.1:p.Asp1869Tyr
NM_001130983.1:c.5575G>T	NP_001124455.1:p.Asp1859Tyr
NM_001130984.1:c.5533G>T	NP_001124456.1:p.Asp1845Tyr
NM_001130985.1:c.5563G>T	NP_001124457.1:p.Asp1855Tyr
NM_001130986.1:c.5470G>T	NP_001124458.1:p.Asp1824Tyr
NM_001130987.1:c.5626G>T	NP_001124459.1:p.Asp1876Tyr
NM_003494.3:c.5509G>T	NP_003485.1:p.Asp1837Tyr
XM_005264584.3:c.5668G>T	XP_005264641.1:p.Asp1890Tyr
XM_005264585.3:c.5665G>T	XP_005264642.1:p.Asp1889Tyr
XM_005264584.4:c.5668G>T	XP_005264641.1:p.Asp1890Tyr
XM_005264585.5:c.5665G>T	XP_005264642.1:p.Asp1889Tyr
NM_001130987.2:c.5626G>T MANE Select	NP_001124459.1:p.Asp1876Tyr
NM_001130455.2:c.5512G>T	NP_001123927.1:p.Asp1838Tyr
NM_001130976.2:c.5467G>T	NP_001124448.1:p.Asp1823Tyr
NM_001130977.2:c.5530G>T	NP_001124449.1:p.Asp1844Tyr
NM_001130978.2:c.5572G>T	NP_001124450.1:p.Asp1858Tyr
NM_001130979.2:c.5602G>T	NP_001124451.1:p.Asp1868Tyr
NM_001130980.2:c.5560G>T	NP_001124452.1:p.Asp1854Tyr
NM_001130981.2:c.5623G>T	NP_001124453.1:p.Asp1875Tyr
NM_001130982.2:c.5605G>T	NP_001124454.1:p.Asp1869Tyr
NM_001130983.2:c.5575G>T	NP_001124455.1:p.Asp1859Tyr
NM_001130984.2:c.5533G>T	NP_001124456.1:p.Asp1845Tyr
NM_001130985.2:c.5563G>T	NP_001124457.1:p.Asp1855Tyr
NM_001130986.2:c.5470G>T	NP_001124458.1:p.Asp1824Tyr
NM_003494.4:c.5509G>T MANE Plus Clinical	NP_003485.1:p.Asp1837Tyr