Canonical Allele Identifier: CA426704732

Gene: DYSF

Linked Data

• MyVariant Identifiers: chr2:g.71906305G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71679175G>A , CM000664.2:g.71679175G>A	GRCh38
NC_000002.11:g.71906305G>A , CM000664.1:g.71906305G>A	GRCh37
NC_000002.10:g.71759813G>A	NCBI36
NG_008694.1:g.230553G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698057.1:c.3417G>A	ENSP00000513536.1:p.Gln1139=
ENST00000698058.1:c.2634G>A	ENSP00000513537.1:p.Gln878=
ENST00000698059.1:c.2742G>A	ENSP00000513538.1:p.Gln914=
ENST00000258104.8:c.5886G>A MANE Plus Clinical	ENSP00000258104.3:p.Gln1962=
ENST00000410020.8:c.6003G>A MANE Select	ENSP00000386881.3:p.Gln2001=
ENST00000258104.7:c.5886G>A	ENSP00000258104.3:p.Gln1962=
ENST00000394120.6:c.5889G>A	ENSP00000377678.2:p.Gln1963=
ENST00000409366.5:c.5952G>A	ENSP00000386512.1:p.Gln1984=
ENST00000409582.7:c.6000G>A	ENSP00000386547.3:p.Gln2000=
ENST00000409651.5:c.5982G>A	ENSP00000386683.1:p.Gln1994=
ENST00000409744.5:c.5910G>A	ENSP00000386285.1:p.Gln1970=
ENST00000409762.5:c.5937G>A	ENSP00000387137.1:p.Gln1979=
ENST00000410020.7:c.6003G>A	ENSP00000386881.3:p.Gln2001=
ENST00000410041.1:c.5940G>A	ENSP00000386617.1:p.Gln1980=
ENST00000413539.6:c.5979G>A	ENSP00000407046.2:p.Gln1993=
ENST00000429174.6:c.5949G>A	ENSP00000398305.2:p.Gln1983=
ENST00000479049.6:n.2771G>A
NM_001130455.1:c.5889G>A	NP_001123927.1:p.Gln1963=
NM_001130976.1:c.5844G>A	NP_001124448.1:p.Gln1948=
NM_001130977.1:c.5907G>A	NP_001124449.1:p.Gln1969=
NM_001130978.1:c.5949G>A	NP_001124450.1:p.Gln1983=
NM_001130979.1:c.5979G>A	NP_001124451.1:p.Gln1993=
NM_001130980.1:c.5937G>A	NP_001124452.1:p.Gln1979=
NM_001130981.1:c.6000G>A	NP_001124453.1:p.Gln2000=
NM_001130982.1:c.5982G>A	NP_001124454.1:p.Gln1994=
NM_001130983.1:c.5952G>A	NP_001124455.1:p.Gln1984=
NM_001130984.1:c.5910G>A	NP_001124456.1:p.Gln1970=
NM_001130985.1:c.5940G>A	NP_001124457.1:p.Gln1980=
NM_001130986.1:c.5847G>A	NP_001124458.1:p.Gln1949=
NM_001130987.1:c.6003G>A	NP_001124459.1:p.Gln2001=
NM_003494.3:c.5886G>A	NP_003485.1:p.Gln1962=
XM_005264584.3:c.6045G>A	XP_005264641.1:p.Gln2015=
XM_005264585.3:c.6042G>A	XP_005264642.1:p.Gln2014=
XM_005264584.4:c.6045G>A	XP_005264641.1:p.Gln2015=
XM_005264585.5:c.6042G>A	XP_005264642.1:p.Gln2014=
NM_001130987.2:c.6003G>A MANE Select	NP_001124459.1:p.Gln2001=
NM_001130455.2:c.5889G>A	NP_001123927.1:p.Gln1963=
NM_001130976.2:c.5844G>A	NP_001124448.1:p.Gln1948=
NM_001130977.2:c.5907G>A	NP_001124449.1:p.Gln1969=
NM_001130978.2:c.5949G>A	NP_001124450.1:p.Gln1983=
NM_001130979.2:c.5979G>A	NP_001124451.1:p.Gln1993=
NM_001130980.2:c.5937G>A	NP_001124452.1:p.Gln1979=
NM_001130981.2:c.6000G>A	NP_001124453.1:p.Gln2000=
NM_001130982.2:c.5982G>A	NP_001124454.1:p.Gln1994=
NM_001130983.2:c.5952G>A	NP_001124455.1:p.Gln1984=
NM_001130984.2:c.5910G>A	NP_001124456.1:p.Gln1970=
NM_001130985.2:c.5940G>A	NP_001124457.1:p.Gln1980=
NM_001130986.2:c.5847G>A	NP_001124458.1:p.Gln1949=
NM_003494.4:c.5886G>A MANE Plus Clinical	NP_003485.1:p.Gln1962=