Canonical Allele Identifier: CA1707158
Community Standard Title: NM_001130987.2(DYSF):c.4858C>T (p.Arg1620Cys)
Gene: DYSF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71658980C>T , CM000664.2:g.71658980C>T GRCh38
NC_000002.11:g.71886110C>T , CM000664.1:g.71886110C>T GRCh37
NC_000002.10:g.71739618C>T NCBI36
NG_008694.1:g.210358C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001130987.2:c.4858C>T MANE Select NP_001124459.1:p.Arg1620Cys
ENST00000410020.8:c.4858C>T MANE Select ENSP00000386881.3:p.Arg1620Cys
NM_003494.4:c.4741C>T MANE Plus Clinical NP_003485.1:p.Arg1581Cys
ENST00000258104.8:c.4741C>T MANE Plus Clinical ENSP00000258104.3:p.Arg1581Cys
NM_001130455.1:c.4744C>T NP_001123927.1:p.Arg1582Cys
NM_001130455.2:c.4744C>T NP_001123927.1:p.Arg1582Cys
NM_001130976.1:c.4699C>T NP_001124448.1:p.Arg1567Cys
NM_001130976.2:c.4699C>T NP_001124448.1:p.Arg1567Cys
NM_001130977.1:c.4762C>T NP_001124449.1:p.Arg1588Cys
NM_001130977.2:c.4762C>T NP_001124449.1:p.Arg1588Cys
NM_001130978.1:c.4804C>T NP_001124450.1:p.Arg1602Cys
NM_001130978.2:c.4804C>T NP_001124450.1:p.Arg1602Cys
NM_001130979.1:c.4834C>T NP_001124451.1:p.Arg1612Cys
NM_001130979.2:c.4834C>T NP_001124451.1:p.Arg1612Cys
NM_001130980.1:c.4792C>T NP_001124452.1:p.Arg1598Cys
NM_001130980.2:c.4792C>T NP_001124452.1:p.Arg1598Cys
NM_001130981.1:c.4855C>T NP_001124453.1:p.Arg1619Cys
NM_001130981.2:c.4855C>T NP_001124453.1:p.Arg1619Cys
NM_001130982.1:c.4837C>T NP_001124454.1:p.Arg1613Cys
NM_001130982.2:c.4837C>T NP_001124454.1:p.Arg1613Cys
NM_001130983.1:c.4807C>T NP_001124455.1:p.Arg1603Cys
NM_001130983.2:c.4807C>T NP_001124455.1:p.Arg1603Cys
NM_001130984.1:c.4765C>T NP_001124456.1:p.Arg1589Cys
NM_001130984.2:c.4765C>T NP_001124456.1:p.Arg1589Cys
NM_001130985.1:c.4795C>T NP_001124457.1:p.Arg1599Cys
NM_001130985.2:c.4795C>T NP_001124457.1:p.Arg1599Cys
NM_001130986.1:c.4702C>T NP_001124458.1:p.Arg1568Cys
NM_001130986.2:c.4702C>T NP_001124458.1:p.Arg1568Cys
NM_001130987.1:c.4858C>T NP_001124459.1:p.Arg1620Cys
NM_003494.3:c.4741C>T NP_003485.1:p.Arg1581Cys
ENST00000258104.7:c.4741C>T ENSP00000258104.3:p.Arg1581Cys
ENST00000394120.6:c.4744C>T ENSP00000377678.2:p.Arg1582Cys
ENST00000409366.5:c.4807C>T ENSP00000386512.1:p.Arg1603Cys
ENST00000409582.7:c.4855C>T ENSP00000386547.3:p.Arg1619Cys
ENST00000409651.5:c.4837C>T ENSP00000386683.1:p.Arg1613Cys
ENST00000409744.5:c.4765C>T ENSP00000386285.1:p.Arg1589Cys
ENST00000409762.5:c.4792C>T ENSP00000387137.1:p.Arg1598Cys
ENST00000410020.7:c.4858C>T ENSP00000386881.3:p.Arg1620Cys
ENST00000410041.1:c.4795C>T ENSP00000386617.1:p.Arg1599Cys
ENST00000413539.6:c.4834C>T ENSP00000407046.2:p.Arg1612Cys
ENST00000429174.6:c.4804C>T ENSP00000398305.2:p.Arg1602Cys
ENST00000479049.6:n.1626C>T
ENST00000698057.1:c.2272C>T ENSP00000513536.1:p.Arg758Cys
ENST00000698058.1:c.1489C>T ENSP00000513537.1:p.Arg497Cys
ENST00000698059.1:c.1597C>T ENSP00000513538.1:p.Arg533Cys
XM_005264584.3:c.4900C>T XP_005264641.1:p.Arg1634Cys
XM_005264584.4:c.4900C>T XP_005264641.1:p.Arg1634Cys
XM_005264585.3:c.4897C>T XP_005264642.1:p.Arg1633Cys
XM_005264585.5:c.4897C>T XP_005264642.1:p.Arg1633Cys
XR_001738969.1:n.5058C>T