Canonical Allele Identifier: CA10576055
Gene: SRC HGNC NCBI

Linked Data

ClinVar Variation Id: 225689
dbSNP Id: rs879255268

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.37403347G>A , CM000682.2:g.37403347G>A GRCh38
NC_000020.10:g.36031750G>A , CM000682.1:g.36031750G>A GRCh37
NC_000020.9:g.35465164G>A NCBI36
NG_023033.1:g.63663G>A , LRG_1018:g.63663G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000358208.9:c.1630G>A ENSP00000350941.5:p.Glu544Lys
ENST00000692112.1:c.1579G>A ENSP00000508666.1:p.Glu527Lys
ENST00000692423.1:c.1579G>A ENSP00000509325.1:p.Glu527Lys
ENST00000373578.7:c.1579G>A MANE Select ENSP00000362680.2:p.Glu527Lys
ENST00000358208.8:c.1579G>A ENSP00000350941.4:p.Glu527Lys
ENST00000373558.2:c.1597G>A ENSP00000362659.2:p.Glu533Lys
ENST00000373567.6:c.1579G>A ENSP00000362668.2:p.Glu527Lys
ENST00000373578.6:c.1579G>A ENSP00000362680.2:p.Glu527Lys
ENST00000477066.5:n.1225G>A
NM_005417.4:c.1579G>A NP_005408.1:p.Glu527Lys
NM_198291.2:c.1579G>A , LRG_1018t1:c.1579G>A NP_938033.1:p.Glu527Lys
XM_011529013.1:c.1579G>A XP_011527315.1:p.Glu527Lys
XM_011529014.1:c.1579G>A XP_011527316.1:p.Glu527Lys
XM_011529013.2:c.1579G>A XP_011527315.1:p.Glu527Lys
XM_017028024.1:c.1597G>A XP_016883513.1:p.Glu533Lys
XM_017028025.1:c.1597G>A XP_016883514.1:p.Glu533Lys
XM_017028026.1:c.1597G>A XP_016883515.1:p.Glu533Lys
XM_017028027.2:c.1597G>A XP_016883516.1:p.Glu533Lys
NM_005417.5:c.1579G>A NP_005408.1:p.Glu527Lys
NM_198291.3:c.1579G>A MANE Select NP_938033.1:p.Glu527Lys