Canonical Allele Identifier: CA635541275

Gene: SRC

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.37394136T>A , CM000682.2:g.37394136T>A	GRCh38
NC_000020.10:g.36022539T>A , CM000682.1:g.36022539T>A	GRCh37
NC_000020.9:g.35455953T>A	NCBI36
NG_023033.1:g.54452T>A , LRG_1018:g.54452T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358208.9:c.501-38T>A	ENSP00000350941.5:n.501-38T>A
ENST00000692112.1:c.450-38T>A	ENSP00000508666.1:n.450-38T>A
ENST00000692423.1:c.450-38T>A	ENSP00000509325.1:n.450-38T>A
ENST00000373578.7:c.450-38T>A MANE Select	ENSP00000362680.2:n.450-38T>A
ENST00000358208.8:c.450-38T>A	ENSP00000350941.4:n.450-38T>A
ENST00000373558.2:c.468-38T>A	ENSP00000362659.2:n.468-38T>A
ENST00000373567.6:c.450-38T>A	ENSP00000362668.2:n.450-38T>A
ENST00000373578.6:c.450-38T>A	ENSP00000362680.2:n.450-38T>A
ENST00000472968.1:n.423T>A
ENST00000489153.1:n.250-38T>A
NM_005417.4:c.450-38T>A	NP_005408.1:n.450-38T>A
NM_198291.2:c.450-38T>A , LRG_1018t1:c.450-38T>A	NP_938033.1:n.450-38T>A
XM_011529013.1:c.450-38T>A	XP_011527315.1:n.450-38T>A
XM_011529014.1:c.450-38T>A	XP_011527316.1:n.450-38T>A
XM_011529013.2:c.450-38T>A	XP_011527315.1:n.450-38T>A
XM_017028024.1:c.468-38T>A	XP_016883513.1:n.468-38T>A
XM_017028025.1:c.468-38T>A	XP_016883514.1:n.468-38T>A
XM_017028026.1:c.468-38T>A	XP_016883515.1:n.468-38T>A
XM_017028027.2:c.468-38T>A	XP_016883516.1:n.468-38T>A
NM_005417.5:c.450-38T>A	NP_005408.1:n.450-38T>A
NM_198291.3:c.450-38T>A MANE Select	NP_938033.1:n.450-38T>A