Canonical Allele Identifier: CA347219957

Gene: DYSF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71660571C>A , CM000664.2:g.71660571C>A	GRCh38
NC_000002.11:g.71887701C>A , CM000664.1:g.71887701C>A	GRCh37
NC_000002.10:g.71741209C>A	NCBI36
NG_008694.1:g.211949C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001130987.2:c.4923C>A MANE Select	NP_001124459.1:p.Tyr1641Ter
ENST00000410020.8:c.4923C>A MANE Select	ENSP00000386881.3:p.Tyr1641Ter
NM_003494.4:c.4806C>A MANE Plus Clinical	NP_003485.1:p.Tyr1602Ter
ENST00000258104.8:c.4806C>A MANE Plus Clinical	ENSP00000258104.3:p.Tyr1602Ter
NM_001130455.1:c.4809C>A	NP_001123927.1:p.Tyr1603Ter
NM_001130455.2:c.4809C>A	NP_001123927.1:p.Tyr1603Ter
NM_001130976.1:c.4764C>A	NP_001124448.1:p.Tyr1588Ter
NM_001130976.2:c.4764C>A	NP_001124448.1:p.Tyr1588Ter
NM_001130977.1:c.4827C>A	NP_001124449.1:p.Tyr1609Ter
NM_001130977.2:c.4827C>A	NP_001124449.1:p.Tyr1609Ter
NM_001130978.1:c.4869C>A	NP_001124450.1:p.Tyr1623Ter
NM_001130978.2:c.4869C>A	NP_001124450.1:p.Tyr1623Ter
NM_001130979.1:c.4899C>A	NP_001124451.1:p.Tyr1633Ter
NM_001130979.2:c.4899C>A	NP_001124451.1:p.Tyr1633Ter
NM_001130980.1:c.4857C>A	NP_001124452.1:p.Tyr1619Ter
NM_001130980.2:c.4857C>A	NP_001124452.1:p.Tyr1619Ter
NM_001130981.1:c.4920C>A	NP_001124453.1:p.Tyr1640Ter
NM_001130981.2:c.4920C>A	NP_001124453.1:p.Tyr1640Ter
NM_001130982.1:c.4902C>A	NP_001124454.1:p.Tyr1634Ter
NM_001130982.2:c.4902C>A	NP_001124454.1:p.Tyr1634Ter
NM_001130983.1:c.4872C>A	NP_001124455.1:p.Tyr1624Ter
NM_001130983.2:c.4872C>A	NP_001124455.1:p.Tyr1624Ter
NM_001130984.1:c.4830C>A	NP_001124456.1:p.Tyr1610Ter
NM_001130984.2:c.4830C>A	NP_001124456.1:p.Tyr1610Ter
NM_001130985.1:c.4860C>A	NP_001124457.1:p.Tyr1620Ter
NM_001130985.2:c.4860C>A	NP_001124457.1:p.Tyr1620Ter
NM_001130986.1:c.4767C>A	NP_001124458.1:p.Tyr1589Ter
NM_001130986.2:c.4767C>A	NP_001124458.1:p.Tyr1589Ter
NM_001130987.1:c.4923C>A	NP_001124459.1:p.Tyr1641Ter
NM_003494.3:c.4806C>A	NP_003485.1:p.Tyr1602Ter
ENST00000258104.7:c.4806C>A	ENSP00000258104.3:p.Tyr1602Ter
ENST00000394120.6:c.4809C>A	ENSP00000377678.2:p.Tyr1603Ter
ENST00000409366.5:c.4872C>A	ENSP00000386512.1:p.Tyr1624Ter
ENST00000409582.7:c.4920C>A	ENSP00000386547.3:p.Tyr1640Ter
ENST00000409651.5:c.4902C>A	ENSP00000386683.1:p.Tyr1634Ter
ENST00000409744.5:c.4830C>A	ENSP00000386285.1:p.Tyr1610Ter
ENST00000409762.5:c.4857C>A	ENSP00000387137.1:p.Tyr1619Ter
ENST00000410020.7:c.4923C>A	ENSP00000386881.3:p.Tyr1641Ter
ENST00000410041.1:c.4860C>A	ENSP00000386617.1:p.Tyr1620Ter
ENST00000413539.6:c.4899C>A	ENSP00000407046.2:p.Tyr1633Ter
ENST00000429174.6:c.4869C>A	ENSP00000398305.2:p.Tyr1623Ter
ENST00000479049.6:n.1691C>A
ENST00000698057.1:c.2337C>A	ENSP00000513536.1:p.Tyr779Ter
ENST00000698058.1:c.1554C>A	ENSP00000513537.1:p.Tyr518Ter
ENST00000698059.1:c.1662C>A	ENSP00000513538.1:p.Tyr554Ter
XM_005264584.3:c.4965C>A	XP_005264641.1:p.Tyr1655Ter
XM_005264584.4:c.4965C>A	XP_005264641.1:p.Tyr1655Ter
XM_005264585.3:c.4962C>A	XP_005264642.1:p.Tyr1654Ter
XM_005264585.5:c.4962C>A	XP_005264642.1:p.Tyr1654Ter
XR_001738969.1:n.5123C>A