Canonical Allele Identifier: CA426701178

Gene: DYSF

Linked Data

• MyVariant Identifiers: chr2:g.71778280A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71551150A>C , CM000664.2:g.71551150A>C	GRCh38
NC_000002.11:g.71778280A>C , CM000664.1:g.71778280A>C	GRCh37
NC_000002.10:g.71631788A>C	NCBI36
NG_008694.1:g.102528A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258104.8:c.1632A>C MANE Plus Clinical	ENSP00000258104.3:p.Thr544=
ENST00000410020.8:c.1686A>C MANE Select	ENSP00000386881.3:p.Thr562=
ENST00000258104.7:c.1632A>C	ENSP00000258104.3:p.Thr544=
ENST00000394120.6:c.1635A>C	ENSP00000377678.2:p.Thr545=
ENST00000409366.5:c.1635A>C	ENSP00000386512.1:p.Thr545=
ENST00000409582.7:c.1683A>C	ENSP00000386547.3:p.Thr561=
ENST00000409651.5:c.1728A>C	ENSP00000386683.1:p.Thr576=
ENST00000409744.5:c.1593A>C	ENSP00000386285.1:p.Thr531=
ENST00000409762.5:c.1683A>C	ENSP00000387137.1:p.Thr561=
ENST00000410020.7:c.1686A>C	ENSP00000386881.3:p.Thr562=
ENST00000410041.1:c.1686A>C	ENSP00000386617.1:p.Thr562=
ENST00000413539.6:c.1725A>C	ENSP00000407046.2:p.Thr575=
ENST00000429174.6:c.1632A>C	ENSP00000398305.2:p.Thr544=
NM_001130455.1:c.1635A>C	NP_001123927.1:p.Thr545=
NM_001130976.1:c.1590A>C	NP_001124448.1:p.Thr530=
NM_001130977.1:c.1590A>C	NP_001124449.1:p.Thr530=
NM_001130978.1:c.1632A>C	NP_001124450.1:p.Thr544=
NM_001130979.1:c.1725A>C	NP_001124451.1:p.Thr575=
NM_001130980.1:c.1683A>C	NP_001124452.1:p.Thr561=
NM_001130981.1:c.1683A>C	NP_001124453.1:p.Thr561=
NM_001130982.1:c.1728A>C	NP_001124454.1:p.Thr576=
NM_001130983.1:c.1635A>C	NP_001124455.1:p.Thr545=
NM_001130984.1:c.1593A>C	NP_001124456.1:p.Thr531=
NM_001130985.1:c.1686A>C	NP_001124457.1:p.Thr562=
NM_001130986.1:c.1593A>C	NP_001124458.1:p.Thr531=
NM_001130987.1:c.1686A>C	NP_001124459.1:p.Thr562=
NM_003494.3:c.1632A>C	NP_003485.1:p.Thr544=
XM_005264584.3:c.1728A>C	XP_005264641.1:p.Thr576=
XM_005264585.3:c.1725A>C	XP_005264642.1:p.Thr575=
XM_005264584.4:c.1728A>C	XP_005264641.1:p.Thr576=
XM_005264585.5:c.1725A>C	XP_005264642.1:p.Thr575=
XR_001738969.1:n.1886A>C
NM_001130987.2:c.1686A>C MANE Select	NP_001124459.1:p.Thr562=
NM_001130455.2:c.1635A>C	NP_001123927.1:p.Thr545=
NM_001130976.2:c.1590A>C	NP_001124448.1:p.Thr530=
NM_001130977.2:c.1590A>C	NP_001124449.1:p.Thr530=
NM_001130978.2:c.1632A>C	NP_001124450.1:p.Thr544=
NM_001130979.2:c.1725A>C	NP_001124451.1:p.Thr575=
NM_001130980.2:c.1683A>C	NP_001124452.1:p.Thr561=
NM_001130981.2:c.1683A>C	NP_001124453.1:p.Thr561=
NM_001130982.2:c.1728A>C	NP_001124454.1:p.Thr576=
NM_001130983.2:c.1635A>C	NP_001124455.1:p.Thr545=
NM_001130984.2:c.1593A>C	NP_001124456.1:p.Thr531=
NM_001130985.2:c.1686A>C	NP_001124457.1:p.Thr562=
NM_001130986.2:c.1593A>C	NP_001124458.1:p.Thr531=
NM_003494.4:c.1632A>C MANE Plus Clinical	NP_003485.1:p.Thr544=