Canonical Allele Identifier: CA347223468

Gene: DYSF

Linked Data

• MyVariant Identifiers: chr2:g.71896755A>T (hg19) ; chr2:g.71669625A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71669625A>T , CM000664.2:g.71669625A>T	GRCh38
NC_000002.11:g.71896755A>T , CM000664.1:g.71896755A>T	GRCh37
NC_000002.10:g.71750263A>T	NCBI36
NG_008694.1:g.221003A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.3077A>T	ENSP00000513536.1:p.Glu1026Val
ENST00000698058.1:c.2294A>T	ENSP00000513537.1:p.Glu765Val
ENST00000698059.1:c.2402A>T	ENSP00000513538.1:p.Glu801Val
ENST00000258104.8:c.5546A>T MANE Plus Clinical	ENSP00000258104.3:p.Glu1849Val
ENST00000410020.8:c.5663A>T MANE Select	ENSP00000386881.3:p.Glu1888Val
ENST00000258104.7:c.5546A>T	ENSP00000258104.3:p.Glu1849Val
ENST00000394120.6:c.5549A>T	ENSP00000377678.2:p.Glu1850Val
ENST00000409366.5:c.5612A>T	ENSP00000386512.1:p.Glu1871Val
ENST00000409582.7:c.5660A>T	ENSP00000386547.3:p.Glu1887Val
ENST00000409651.5:c.5642A>T	ENSP00000386683.1:p.Glu1881Val
ENST00000409744.5:c.5570A>T	ENSP00000386285.1:p.Glu1857Val
ENST00000409762.5:c.5597A>T	ENSP00000387137.1:p.Glu1866Val
ENST00000410020.7:c.5663A>T	ENSP00000386881.3:p.Glu1888Val
ENST00000410041.1:c.5600A>T	ENSP00000386617.1:p.Glu1867Val
ENST00000413539.6:c.5639A>T	ENSP00000407046.2:p.Glu1880Val
ENST00000429174.6:c.5609A>T	ENSP00000398305.2:p.Glu1870Val
ENST00000479049.6:n.2431A>T
NM_001130455.1:c.5549A>T	NP_001123927.1:p.Glu1850Val
NM_001130976.1:c.5504A>T	NP_001124448.1:p.Glu1835Val
NM_001130977.1:c.5567A>T	NP_001124449.1:p.Glu1856Val
NM_001130978.1:c.5609A>T	NP_001124450.1:p.Glu1870Val
NM_001130979.1:c.5639A>T	NP_001124451.1:p.Glu1880Val
NM_001130980.1:c.5597A>T	NP_001124452.1:p.Glu1866Val
NM_001130981.1:c.5660A>T	NP_001124453.1:p.Glu1887Val
NM_001130982.1:c.5642A>T	NP_001124454.1:p.Glu1881Val
NM_001130983.1:c.5612A>T	NP_001124455.1:p.Glu1871Val
NM_001130984.1:c.5570A>T	NP_001124456.1:p.Glu1857Val
NM_001130985.1:c.5600A>T	NP_001124457.1:p.Glu1867Val
NM_001130986.1:c.5507A>T	NP_001124458.1:p.Glu1836Val
NM_001130987.1:c.5663A>T	NP_001124459.1:p.Glu1888Val
NM_003494.3:c.5546A>T	NP_003485.1:p.Glu1849Val
XM_005264584.3:c.5705A>T	XP_005264641.1:p.Glu1902Val
XM_005264585.3:c.5702A>T	XP_005264642.1:p.Glu1901Val
XM_005264584.4:c.5705A>T	XP_005264641.1:p.Glu1902Val
XM_005264585.5:c.5702A>T	XP_005264642.1:p.Glu1901Val
NM_001130987.2:c.5663A>T MANE Select	NP_001124459.1:p.Glu1888Val
NM_001130455.2:c.5549A>T	NP_001123927.1:p.Glu1850Val
NM_001130976.2:c.5504A>T	NP_001124448.1:p.Glu1835Val
NM_001130977.2:c.5567A>T	NP_001124449.1:p.Glu1856Val
NM_001130978.2:c.5609A>T	NP_001124450.1:p.Glu1870Val
NM_001130979.2:c.5639A>T	NP_001124451.1:p.Glu1880Val
NM_001130980.2:c.5597A>T	NP_001124452.1:p.Glu1866Val
NM_001130981.2:c.5660A>T	NP_001124453.1:p.Glu1887Val
NM_001130982.2:c.5642A>T	NP_001124454.1:p.Glu1881Val
NM_001130983.2:c.5612A>T	NP_001124455.1:p.Glu1871Val
NM_001130984.2:c.5570A>T	NP_001124456.1:p.Glu1857Val
NM_001130985.2:c.5600A>T	NP_001124457.1:p.Glu1867Val
NM_001130986.2:c.5507A>T	NP_001124458.1:p.Glu1836Val
NM_003494.4:c.5546A>T MANE Plus Clinical	NP_003485.1:p.Glu1849Val