Canonical Allele Identifier: CA1260140076
Gene: DYSF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71643993A= , CM000664.2:g.71643993A= GRCh38
NC_000002.11:g.71871123A= , CM000664.1:g.71871123A= GRCh37
NC_000002.10:g.71724631A= NCBI36
NG_008694.1:g.195371A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698057.1:c.1970A= ENSP00000513536.1:p.Lys657=
ENST00000698058.1:c.1187A= ENSP00000513537.1:p.Lys396=
ENST00000698059.1:c.1295A= ENSP00000513538.1:p.Lys432=
ENST00000258104.8:c.4439A= MANE Plus Clinical ENSP00000258104.3:p.Lys1480=
ENST00000410020.8:c.4556A= MANE Select ENSP00000386881.3:p.Lys1519=
ENST00000258104.7:c.4439A= ENSP00000258104.3:p.Lys1480=
ENST00000394120.6:c.4442A= ENSP00000377678.2:p.Lys1481=
ENST00000409366.5:c.4505A= ENSP00000386512.1:p.Lys1502=
ENST00000409582.7:c.4553A= ENSP00000386547.3:p.Lys1518=
ENST00000409651.5:c.4535A= ENSP00000386683.1:p.Lys1512=
ENST00000409744.5:c.4463A= ENSP00000386285.1:p.Lys1488=
ENST00000409762.5:c.4490A= ENSP00000387137.1:p.Lys1497=
ENST00000410020.7:c.4556A= ENSP00000386881.3:p.Lys1519=
ENST00000410041.1:c.4493A= ENSP00000386617.1:p.Lys1498=
ENST00000413539.6:c.4532A= ENSP00000407046.2:p.Lys1511=
ENST00000429174.6:c.4502A= ENSP00000398305.2:p.Lys1501=
ENST00000468173.1:n.738A=
ENST00000479049.6:n.1324A=
NM_001130455.1:c.4442A= NP_001123927.1:p.Lys1481=
NM_001130976.1:c.4397A= NP_001124448.1:p.Lys1466=
NM_001130977.1:c.4460A= NP_001124449.1:p.Lys1487=
NM_001130978.1:c.4502A= NP_001124450.1:p.Lys1501=
NM_001130979.1:c.4532A= NP_001124451.1:p.Lys1511=
NM_001130980.1:c.4490A= NP_001124452.1:p.Lys1497=
NM_001130981.1:c.4553A= NP_001124453.1:p.Lys1518=
NM_001130982.1:c.4535A= NP_001124454.1:p.Lys1512=
NM_001130983.1:c.4505A= NP_001124455.1:p.Lys1502=
NM_001130984.1:c.4463A= NP_001124456.1:p.Lys1488=
NM_001130985.1:c.4493A= NP_001124457.1:p.Lys1498=
NM_001130986.1:c.4400A= NP_001124458.1:p.Lys1467=
NM_001130987.1:c.4556A= NP_001124459.1:p.Lys1519=
NM_003494.3:c.4439A= NP_003485.1:p.Lys1480=
XM_005264584.3:c.4598A= XP_005264641.1:p.Lys1533=
XM_005264585.3:c.4595A= XP_005264642.1:p.Lys1532=
XM_005264584.4:c.4598A= XP_005264641.1:p.Lys1533=
XM_005264585.5:c.4595A= XP_005264642.1:p.Lys1532=
XR_001738969.1:n.4756A=
NM_001130987.2:c.4556A= MANE Select NP_001124459.1:p.Lys1519=
NM_001130455.2:c.4442A= NP_001123927.1:p.Lys1481=
NM_001130976.2:c.4397A= NP_001124448.1:p.Lys1466=
NM_001130977.2:c.4460A= NP_001124449.1:p.Lys1487=
NM_001130978.2:c.4502A= NP_001124450.1:p.Lys1501=
NM_001130979.2:c.4532A= NP_001124451.1:p.Lys1511=
NM_001130980.2:c.4490A= NP_001124452.1:p.Lys1497=
NM_001130981.2:c.4553A= NP_001124453.1:p.Lys1518=
NM_001130982.2:c.4535A= NP_001124454.1:p.Lys1512=
NM_001130983.2:c.4505A= NP_001124455.1:p.Lys1502=
NM_001130984.2:c.4463A= NP_001124456.1:p.Lys1488=
NM_001130985.2:c.4493A= NP_001124457.1:p.Lys1498=
NM_001130986.2:c.4400A= NP_001124458.1:p.Lys1467=
NM_003494.4:c.4439A= MANE Plus Clinical NP_003485.1:p.Lys1480=