Canonical Allele Identifier: CA1706362
Gene: DYSF HGNC NCBI

Linked Data

ClinVar Variation Id: 499191
dbSNP Id: rs142404822
gnomAD v2: 2-71797361-C-T
gnomAD v3: 2-71570231-C-T
gnomAD v4: 2-71570231-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.71570231C>T , CM000664.2:g.71570231C>T GRCh38
NC_000002.11:g.71797361C>T , CM000664.1:g.71797361C>T GRCh37
NC_000002.10:g.71650869C>T NCBI36
NG_008694.1:g.121609C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698057.1:c.354C>T ENSP00000513536.1:p.Asn118=
ENST00000258104.8:c.2928C>T MANE Plus Clinical ENSP00000258104.3:p.Asn976=
ENST00000410020.8:c.2982C>T MANE Select ENSP00000386881.3:p.Asn994=
ENST00000258104.7:c.2928C>T ENSP00000258104.3:p.Asn976=
ENST00000394120.6:c.2931C>T ENSP00000377678.2:p.Asn977=
ENST00000409366.5:c.2931C>T ENSP00000386512.1:p.Asn977=
ENST00000409582.7:c.2979C>T ENSP00000386547.3:p.Asn993=
ENST00000409651.5:c.3024C>T ENSP00000386683.1:p.Asn1008=
ENST00000409744.5:c.2889C>T ENSP00000386285.1:p.Asn963=
ENST00000409762.5:c.2979C>T ENSP00000387137.1:p.Asn993=
ENST00000410020.7:c.2982C>T ENSP00000386881.3:p.Asn994=
ENST00000410041.1:c.2982C>T ENSP00000386617.1:p.Asn994=
ENST00000413539.6:c.3021C>T ENSP00000407046.2:p.Asn1007=
ENST00000429174.6:c.2928C>T ENSP00000398305.2:p.Asn976=
ENST00000461565.1:n.94C>T
NM_001130455.1:c.2931C>T NP_001123927.1:p.Asn977=
NM_001130976.1:c.2886C>T NP_001124448.1:p.Asn962=
NM_001130977.1:c.2886C>T NP_001124449.1:p.Asn962=
NM_001130978.1:c.2928C>T NP_001124450.1:p.Asn976=
NM_001130979.1:c.3021C>T NP_001124451.1:p.Asn1007=
NM_001130980.1:c.2979C>T NP_001124452.1:p.Asn993=
NM_001130981.1:c.2979C>T NP_001124453.1:p.Asn993=
NM_001130982.1:c.3024C>T NP_001124454.1:p.Asn1008=
NM_001130983.1:c.2931C>T NP_001124455.1:p.Asn977=
NM_001130984.1:c.2889C>T NP_001124456.1:p.Asn963=
NM_001130985.1:c.2982C>T NP_001124457.1:p.Asn994=
NM_001130986.1:c.2889C>T NP_001124458.1:p.Asn963=
NM_001130987.1:c.2982C>T NP_001124459.1:p.Asn994=
NM_003494.3:c.2928C>T NP_003485.1:p.Asn976=
XM_005264584.3:c.3024C>T XP_005264641.1:p.Asn1008=
XM_005264585.3:c.3021C>T XP_005264642.1:p.Asn1007=
XM_005264584.4:c.3024C>T XP_005264641.1:p.Asn1008=
XM_005264585.5:c.3021C>T XP_005264642.1:p.Asn1007=
XR_001738969.1:n.3182C>T
NM_001130987.2:c.2982C>T MANE Select NP_001124459.1:p.Asn994=
NM_001130455.2:c.2931C>T NP_001123927.1:p.Asn977=
NM_001130976.2:c.2886C>T NP_001124448.1:p.Asn962=
NM_001130977.2:c.2886C>T NP_001124449.1:p.Asn962=
NM_001130978.2:c.2928C>T NP_001124450.1:p.Asn976=
NM_001130979.2:c.3021C>T NP_001124451.1:p.Asn1007=
NM_001130980.2:c.2979C>T NP_001124452.1:p.Asn993=
NM_001130981.2:c.2979C>T NP_001124453.1:p.Asn993=
NM_001130982.2:c.3024C>T NP_001124454.1:p.Asn1008=
NM_001130983.2:c.2931C>T NP_001124455.1:p.Asn977=
NM_001130984.2:c.2889C>T NP_001124456.1:p.Asn963=
NM_001130985.2:c.2982C>T NP_001124457.1:p.Asn994=
NM_001130986.2:c.2889C>T NP_001124458.1:p.Asn963=
NM_003494.4:c.2928C>T MANE Plus Clinical NP_003485.1:p.Asn976=