Canonical Allele Identifier: CA1260124028
Gene: DYSF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71611308C= , CM000664.2:g.71611308C= GRCh38
NC_000002.11:g.71838438C= , CM000664.1:g.71838438C= GRCh37
NC_000002.10:g.71691946C= NCBI36
NG_008694.1:g.162686C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698057.1:c.1435C= ENSP00000513536.1:p.Gln479=
ENST00000698058.1:c.652C= ENSP00000513537.1:p.Gln218=
ENST00000698059.1:c.610C= ENSP00000513538.1:p.Gln204=
ENST00000258104.8:c.3967C= MANE Plus Clinical ENSP00000258104.3:p.Gln1323=
ENST00000410020.8:c.4021C= MANE Select ENSP00000386881.3:p.Gln1341=
ENST00000258104.7:c.3967C= ENSP00000258104.3:p.Gln1323=
ENST00000394120.6:c.3970C= ENSP00000377678.2:p.Gln1324=
ENST00000409366.5:c.3970C= ENSP00000386512.1:p.Gln1324=
ENST00000409582.7:c.4018C= ENSP00000386547.3:p.Gln1340=
ENST00000409651.5:c.4063C= ENSP00000386683.1:p.Gln1355=
ENST00000409744.5:c.3928C= ENSP00000386285.1:p.Gln1310=
ENST00000409762.5:c.4018C= ENSP00000387137.1:p.Gln1340=
ENST00000410020.7:c.4021C= ENSP00000386881.3:p.Gln1341=
ENST00000410041.1:c.4021C= ENSP00000386617.1:p.Gln1341=
ENST00000413539.6:c.4060C= ENSP00000407046.2:p.Gln1354=
ENST00000429174.6:c.3967C= ENSP00000398305.2:p.Gln1323=
ENST00000468173.1:n.203C=
ENST00000472873.5:n.351C=
ENST00000479049.6:n.852C=
ENST00000487180.5:n.186C=
ENST00000494501.5:n.327C=
NM_001130455.1:c.3970C= NP_001123927.1:p.Gln1324=
NM_001130976.1:c.3925C= NP_001124448.1:p.Gln1309=
NM_001130977.1:c.3925C= NP_001124449.1:p.Gln1309=
NM_001130978.1:c.3967C= NP_001124450.1:p.Gln1323=
NM_001130979.1:c.4060C= NP_001124451.1:p.Gln1354=
NM_001130980.1:c.4018C= NP_001124452.1:p.Gln1340=
NM_001130981.1:c.4018C= NP_001124453.1:p.Gln1340=
NM_001130982.1:c.4063C= NP_001124454.1:p.Gln1355=
NM_001130983.1:c.3970C= NP_001124455.1:p.Gln1324=
NM_001130984.1:c.3928C= NP_001124456.1:p.Gln1310=
NM_001130985.1:c.4021C= NP_001124457.1:p.Gln1341=
NM_001130986.1:c.3928C= NP_001124458.1:p.Gln1310=
NM_001130987.1:c.4021C= NP_001124459.1:p.Gln1341=
NM_003494.3:c.3967C= NP_003485.1:p.Gln1323=
XM_005264584.3:c.4063C= XP_005264641.1:p.Gln1355=
XM_005264585.3:c.4060C= XP_005264642.1:p.Gln1354=
XM_005264584.4:c.4063C= XP_005264641.1:p.Gln1355=
XM_005264585.5:c.4060C= XP_005264642.1:p.Gln1354=
XR_001738969.1:n.4221C=
NM_001130987.2:c.4021C= MANE Select NP_001124459.1:p.Gln1341=
NM_001130455.2:c.3970C= NP_001123927.1:p.Gln1324=
NM_001130976.2:c.3925C= NP_001124448.1:p.Gln1309=
NM_001130977.2:c.3925C= NP_001124449.1:p.Gln1309=
NM_001130978.2:c.3967C= NP_001124450.1:p.Gln1323=
NM_001130979.2:c.4060C= NP_001124451.1:p.Gln1354=
NM_001130980.2:c.4018C= NP_001124452.1:p.Gln1340=
NM_001130981.2:c.4018C= NP_001124453.1:p.Gln1340=
NM_001130982.2:c.4063C= NP_001124454.1:p.Gln1355=
NM_001130983.2:c.3970C= NP_001124455.1:p.Gln1324=
NM_001130984.2:c.3928C= NP_001124456.1:p.Gln1310=
NM_001130985.2:c.4021C= NP_001124457.1:p.Gln1341=
NM_001130986.2:c.3928C= NP_001124458.1:p.Gln1310=
NM_003494.4:c.3967C= MANE Plus Clinical NP_003485.1:p.Gln1323=