Canonical Allele Identifier: CA426704476

Gene: DYSF

Linked Data

• MyVariant Identifiers: chr2:g.71896756A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71669626A>G , CM000664.2:g.71669626A>G	GRCh38
NC_000002.11:g.71896756A>G , CM000664.1:g.71896756A>G	GRCh37
NC_000002.10:g.71750264A>G	NCBI36
NG_008694.1:g.221004A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698057.1:c.3078A>G	ENSP00000513536.1:p.Glu1026=
ENST00000698058.1:c.2295A>G	ENSP00000513537.1:p.Glu765=
ENST00000698059.1:c.2403A>G	ENSP00000513538.1:p.Glu801=
ENST00000258104.8:c.5547A>G MANE Plus Clinical	ENSP00000258104.3:p.Glu1849=
ENST00000410020.8:c.5664A>G MANE Select	ENSP00000386881.3:p.Glu1888=
ENST00000258104.7:c.5547A>G	ENSP00000258104.3:p.Glu1849=
ENST00000394120.6:c.5550A>G	ENSP00000377678.2:p.Glu1850=
ENST00000409366.5:c.5613A>G	ENSP00000386512.1:p.Glu1871=
ENST00000409582.7:c.5661A>G	ENSP00000386547.3:p.Glu1887=
ENST00000409651.5:c.5643A>G	ENSP00000386683.1:p.Glu1881=
ENST00000409744.5:c.5571A>G	ENSP00000386285.1:p.Glu1857=
ENST00000409762.5:c.5598A>G	ENSP00000387137.1:p.Glu1866=
ENST00000410020.7:c.5664A>G	ENSP00000386881.3:p.Glu1888=
ENST00000410041.1:c.5601A>G	ENSP00000386617.1:p.Glu1867=
ENST00000413539.6:c.5640A>G	ENSP00000407046.2:p.Glu1880=
ENST00000429174.6:c.5610A>G	ENSP00000398305.2:p.Glu1870=
ENST00000479049.6:n.2432A>G
NM_001130455.1:c.5550A>G	NP_001123927.1:p.Glu1850=
NM_001130976.1:c.5505A>G	NP_001124448.1:p.Glu1835=
NM_001130977.1:c.5568A>G	NP_001124449.1:p.Glu1856=
NM_001130978.1:c.5610A>G	NP_001124450.1:p.Glu1870=
NM_001130979.1:c.5640A>G	NP_001124451.1:p.Glu1880=
NM_001130980.1:c.5598A>G	NP_001124452.1:p.Glu1866=
NM_001130981.1:c.5661A>G	NP_001124453.1:p.Glu1887=
NM_001130982.1:c.5643A>G	NP_001124454.1:p.Glu1881=
NM_001130983.1:c.5613A>G	NP_001124455.1:p.Glu1871=
NM_001130984.1:c.5571A>G	NP_001124456.1:p.Glu1857=
NM_001130985.1:c.5601A>G	NP_001124457.1:p.Glu1867=
NM_001130986.1:c.5508A>G	NP_001124458.1:p.Glu1836=
NM_001130987.1:c.5664A>G	NP_001124459.1:p.Glu1888=
NM_003494.3:c.5547A>G	NP_003485.1:p.Glu1849=
XM_005264584.3:c.5706A>G	XP_005264641.1:p.Glu1902=
XM_005264585.3:c.5703A>G	XP_005264642.1:p.Glu1901=
XM_005264584.4:c.5706A>G	XP_005264641.1:p.Glu1902=
XM_005264585.5:c.5703A>G	XP_005264642.1:p.Glu1901=
NM_001130987.2:c.5664A>G MANE Select	NP_001124459.1:p.Glu1888=
NM_001130455.2:c.5550A>G	NP_001123927.1:p.Glu1850=
NM_001130976.2:c.5505A>G	NP_001124448.1:p.Glu1835=
NM_001130977.2:c.5568A>G	NP_001124449.1:p.Glu1856=
NM_001130978.2:c.5610A>G	NP_001124450.1:p.Glu1870=
NM_001130979.2:c.5640A>G	NP_001124451.1:p.Glu1880=
NM_001130980.2:c.5598A>G	NP_001124452.1:p.Glu1866=
NM_001130981.2:c.5661A>G	NP_001124453.1:p.Glu1887=
NM_001130982.2:c.5643A>G	NP_001124454.1:p.Glu1881=
NM_001130983.2:c.5613A>G	NP_001124455.1:p.Glu1871=
NM_001130984.2:c.5571A>G	NP_001124456.1:p.Glu1857=
NM_001130985.2:c.5601A>G	NP_001124457.1:p.Glu1867=
NM_001130986.2:c.5508A>G	NP_001124458.1:p.Glu1836=
NM_003494.4:c.5547A>G MANE Plus Clinical	NP_003485.1:p.Glu1849=