Canonical Allele Identifier: CA16621750
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 425203
ClinVar RCV Id: RCV000488297
dbSNP Id: rs1064797253

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71664399del , CM000664.2:g.71664399del GRCh38
NC_000002.11:g.71891529del , CM000664.1:g.71891529del GRCh37
NC_000002.10:g.71745037del NCBI36
NG_008694.1:g.215777del

Transcript Alleles

HGVS Amino-acid change
ENST00000698057.1:c.2549del ENSP00000513536.1:p.Lys850SerfsTer?
ENST00000698058.1:c.1766del ENSP00000513537.1:p.Lys589SerfsTer?
ENST00000698059.1:c.1874del ENSP00000513538.1:p.Lys625SerfsTer?
ENST00000258104.8:c.5018del MANE Plus Clinical ENSP00000258104.3:p.Lys1673SerfsTer?
ENST00000410020.8:c.5135del MANE Select ENSP00000386881.3:p.Lys1712SerfsTer?
ENST00000258104.7:c.5018del ENSP00000258104.3:p.Lys1673SerfsTer?
ENST00000394120.6:c.5021del ENSP00000377678.2:p.Lys1674SerfsTer?
ENST00000409366.5:c.5084del ENSP00000386512.1:p.Lys1695SerfsTer?
ENST00000409582.7:c.5132del ENSP00000386547.3:p.Lys1711SerfsTer?
ENST00000409651.5:c.5114del ENSP00000386683.1:p.Lys1705SerfsTer?
ENST00000409744.5:c.5042del ENSP00000386285.1:p.Lys1681SerfsTer?
ENST00000409762.5:c.5069del ENSP00000387137.1:p.Lys1690SerfsTer?
ENST00000410020.7:c.5135del ENSP00000386881.3:p.Lys1712SerfsTer?
ENST00000410041.1:c.5072del ENSP00000386617.1:p.Lys1691SerfsTer?
ENST00000413539.6:c.5111del ENSP00000407046.2:p.Lys1704SerfsTer?
ENST00000429174.6:c.5081del ENSP00000398305.2:p.Lys1694SerfsTer?
ENST00000479049.6:n.1903del
NM_001130455.1:c.5021del NP_001123927.1:p.Lys1674SerfsTer?
NM_001130976.1:c.4976del NP_001124448.1:p.Lys1659SerfsTer?
NM_001130977.1:c.5039del NP_001124449.1:p.Lys1680SerfsTer?
NM_001130978.1:c.5081del NP_001124450.1:p.Lys1694SerfsTer?
NM_001130979.1:c.5111del NP_001124451.1:p.Lys1704SerfsTer?
NM_001130980.1:c.5069del NP_001124452.1:p.Lys1690SerfsTer?
NM_001130981.1:c.5132del NP_001124453.1:p.Lys1711SerfsTer?
NM_001130982.1:c.5114del NP_001124454.1:p.Lys1705SerfsTer?
NM_001130983.1:c.5084del NP_001124455.1:p.Lys1695SerfsTer?
NM_001130984.1:c.5042del NP_001124456.1:p.Lys1681SerfsTer?
NM_001130985.1:c.5072del NP_001124457.1:p.Lys1691SerfsTer?
NM_001130986.1:c.4979del NP_001124458.1:p.Lys1660SerfsTer?
NM_001130987.1:c.5135del NP_001124459.1:p.Lys1712SerfsTer?
NM_003494.3:c.5018del NP_003485.1:p.Lys1673SerfsTer?
XM_005264584.3:c.5177del XP_005264641.1:p.Lys1726SerfsTer?
XM_005264585.3:c.5174del XP_005264642.1:p.Lys1725SerfsTer?
XM_005264584.4:c.5177del XP_005264641.1:p.Lys1726SerfsTer?
XM_005264585.5:c.5174del XP_005264642.1:p.Lys1725SerfsTer?
XR_001738969.1:n.5335del
NM_001130987.2:c.5135del MANE Select NP_001124459.1:p.Lys1712SerfsTer?
NM_001130455.2:c.5021del NP_001123927.1:p.Lys1674SerfsTer?
NM_001130976.2:c.4976del NP_001124448.1:p.Lys1659SerfsTer?
NM_001130977.2:c.5039del NP_001124449.1:p.Lys1680SerfsTer?
NM_001130978.2:c.5081del NP_001124450.1:p.Lys1694SerfsTer?
NM_001130979.2:c.5111del NP_001124451.1:p.Lys1704SerfsTer?
NM_001130980.2:c.5069del NP_001124452.1:p.Lys1690SerfsTer?
NM_001130981.2:c.5132del NP_001124453.1:p.Lys1711SerfsTer?
NM_001130982.2:c.5114del NP_001124454.1:p.Lys1705SerfsTer?
NM_001130983.2:c.5084del NP_001124455.1:p.Lys1695SerfsTer?
NM_001130984.2:c.5042del NP_001124456.1:p.Lys1681SerfsTer?
NM_001130985.2:c.5072del NP_001124457.1:p.Lys1691SerfsTer?
NM_001130986.2:c.4979del NP_001124458.1:p.Lys1660SerfsTer?
NM_003494.4:c.5018del MANE Plus Clinical NP_003485.1:p.Lys1673SerfsTer?