Canonical Allele Identifier: CA1260094749

Gene: DYSF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71551137_71551138delinsCA , CM000664.2:g.71551137_71551138delinsCA	GRCh38
NC_000002.11:g.71778267_71778268delinsCA , CM000664.1:g.71778267_71778268delinsCA	GRCh37
NC_000002.10:g.71631775_71631776delinsCA	NCBI36
NG_008694.1:g.102515_102516delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258104.8:c.1619_1620delinsCA MANE Plus Clinical	ENSP00000258104.3:p.Thr540=
ENST00000410020.8:c.1673_1674delinsCA MANE Select	ENSP00000386881.3:p.Thr558=
ENST00000258104.7:c.1619_1620delinsCA	ENSP00000258104.3:p.Thr540=
ENST00000394120.6:c.1622_1623delinsCA	ENSP00000377678.2:p.Thr541=
ENST00000409366.5:c.1622_1623delinsCA	ENSP00000386512.1:p.Thr541=
ENST00000409582.7:c.1670_1671delinsCA	ENSP00000386547.3:p.Thr557=
ENST00000409651.5:c.1715_1716delinsCA	ENSP00000386683.1:p.Thr572=
ENST00000409744.5:c.1580_1581delinsCA	ENSP00000386285.1:p.Thr527=
ENST00000409762.5:c.1670_1671delinsCA	ENSP00000387137.1:p.Thr557=
ENST00000410020.7:c.1673_1674delinsCA	ENSP00000386881.3:p.Thr558=
ENST00000410041.1:c.1673_1674delinsCA	ENSP00000386617.1:p.Thr558=
ENST00000413539.6:c.1712_1713delinsCA	ENSP00000407046.2:p.Thr571=
ENST00000429174.6:c.1619_1620delinsCA	ENSP00000398305.2:p.Thr540=
NM_001130455.1:c.1622_1623delinsCA	NP_001123927.1:p.Thr541=
NM_001130976.1:c.1577_1578delinsCA	NP_001124448.1:p.Thr526=
NM_001130977.1:c.1577_1578delinsCA	NP_001124449.1:p.Thr526=
NM_001130978.1:c.1619_1620delinsCA	NP_001124450.1:p.Thr540=
NM_001130979.1:c.1712_1713delinsCA	NP_001124451.1:p.Thr571=
NM_001130980.1:c.1670_1671delinsCA	NP_001124452.1:p.Thr557=
NM_001130981.1:c.1670_1671delinsCA	NP_001124453.1:p.Thr557=
NM_001130982.1:c.1715_1716delinsCA	NP_001124454.1:p.Thr572=
NM_001130983.1:c.1622_1623delinsCA	NP_001124455.1:p.Thr541=
NM_001130984.1:c.1580_1581delinsCA	NP_001124456.1:p.Thr527=
NM_001130985.1:c.1673_1674delinsCA	NP_001124457.1:p.Thr558=
NM_001130986.1:c.1580_1581delinsCA	NP_001124458.1:p.Thr527=
NM_001130987.1:c.1673_1674delinsCA	NP_001124459.1:p.Thr558=
NM_003494.3:c.1619_1620delinsCA	NP_003485.1:p.Thr540=
XM_005264584.3:c.1715_1716delinsCA	XP_005264641.1:p.Thr572=
XM_005264585.3:c.1712_1713delinsCA	XP_005264642.1:p.Thr571=
XM_005264584.4:c.1715_1716delinsCA	XP_005264641.1:p.Thr572=
XM_005264585.5:c.1712_1713delinsCA	XP_005264642.1:p.Thr571=
XR_001738969.1:n.1873_1874delinsCA
NM_001130987.2:c.1673_1674delinsCA MANE Select	NP_001124459.1:p.Thr558=
NM_001130455.2:c.1622_1623delinsCA	NP_001123927.1:p.Thr541=
NM_001130976.2:c.1577_1578delinsCA	NP_001124448.1:p.Thr526=
NM_001130977.2:c.1577_1578delinsCA	NP_001124449.1:p.Thr526=
NM_001130978.2:c.1619_1620delinsCA	NP_001124450.1:p.Thr540=
NM_001130979.2:c.1712_1713delinsCA	NP_001124451.1:p.Thr571=
NM_001130980.2:c.1670_1671delinsCA	NP_001124452.1:p.Thr557=
NM_001130981.2:c.1670_1671delinsCA	NP_001124453.1:p.Thr557=
NM_001130982.2:c.1715_1716delinsCA	NP_001124454.1:p.Thr572=
NM_001130983.2:c.1622_1623delinsCA	NP_001124455.1:p.Thr541=
NM_001130984.2:c.1580_1581delinsCA	NP_001124456.1:p.Thr527=
NM_001130985.2:c.1673_1674delinsCA	NP_001124457.1:p.Thr558=
NM_001130986.2:c.1580_1581delinsCA	NP_001124458.1:p.Thr527=
NM_003494.4:c.1619_1620delinsCA MANE Plus Clinical	NP_003485.1:p.Thr540=