Canonical Allele Identifier: CA314457756

Gene: SRC

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.37387840T>C , CM000682.2:g.37387840T>C	GRCh38
NC_000020.10:g.36016243T>C , CM000682.1:g.36016243T>C	GRCh37
NC_000020.9:g.35449657T>C	NCBI36
NG_023033.1:g.48156T>C , LRG_1018:g.48156T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358208.9:c.368+1363T>C	ENSP00000350941.5:n.368+1363T>C
ENST00000692112.1:c.350+1666T>C	ENSP00000508666.1:n.350+1666T>C
ENST00000692423.1:c.350+1666T>C	ENSP00000509325.1:n.350+1666T>C
ENST00000373578.7:c.350+1666T>C MANE Select	ENSP00000362680.2:n.350+1666T>C
ENST00000358208.8:c.350+1666T>C	ENSP00000350941.4:n.350+1666T>C
ENST00000373558.2:c.368+1363T>C	ENSP00000362659.2:n.368+1363T>C
ENST00000373567.6:c.350+1666T>C	ENSP00000362668.2:n.350+1666T>C
ENST00000373578.6:c.350+1666T>C	ENSP00000362680.2:n.350+1666T>C
ENST00000472968.1:n.181+1666T>C
NM_005417.4:c.350+1666T>C	NP_005408.1:n.350+1666T>C
NM_198291.2:c.350+1666T>C , LRG_1018t1:c.350+1666T>C	NP_938033.1:n.350+1666T>C
XM_011529013.1:c.350+1666T>C	XP_011527315.1:n.350+1666T>C
XM_011529014.1:c.350+1666T>C	XP_011527316.1:n.350+1666T>C
XM_011529013.2:c.350+1666T>C	XP_011527315.1:n.350+1666T>C
XM_017028024.1:c.368+1363T>C	XP_016883513.1:n.368+1363T>C
XM_017028025.1:c.368+1363T>C	XP_016883514.1:n.368+1363T>C
XM_017028026.1:c.368+1363T>C	XP_016883515.1:n.368+1363T>C
XM_017028027.2:c.368+1363T>C	XP_016883516.1:n.368+1363T>C
NM_005417.5:c.350+1666T>C	NP_005408.1:n.350+1666T>C
NM_198291.3:c.350+1666T>C MANE Select	NP_938033.1:n.350+1666T>C