Canonical Allele Identifier: CA2652768686

Gene: SRC

Linked Data

• gnomAD v4: 20-37393659-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.37393659T>C , CM000682.2:g.37393659T>C	GRCh38
NC_000020.10:g.36022062T>C , CM000682.1:g.36022062T>C	GRCh37
NC_000020.9:g.35455476T>C	NCBI36
NG_023033.1:g.53975T>C , LRG_1018:g.53975T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358208.9:c.402-236T>C	ENSP00000350941.5:n.402-236T>C
ENST00000692112.1:c.351-236T>C	ENSP00000508666.1:n.351-236T>C
ENST00000692423.1:c.351-236T>C	ENSP00000509325.1:n.351-236T>C
ENST00000373578.7:c.351-236T>C MANE Select	ENSP00000362680.2:n.351-236T>C
ENST00000358208.8:c.351-236T>C	ENSP00000350941.4:n.351-236T>C
ENST00000373558.2:c.369-236T>C	ENSP00000362659.2:n.369-236T>C
ENST00000373567.6:c.351-236T>C	ENSP00000362668.2:n.351-236T>C
ENST00000373578.6:c.351-236T>C	ENSP00000362680.2:n.351-236T>C
ENST00000472968.1:n.182-236T>C
NM_005417.4:c.351-236T>C	NP_005408.1:n.351-236T>C
NM_198291.2:c.351-236T>C , LRG_1018t1:c.351-236T>C	NP_938033.1:n.351-236T>C
XM_011529013.1:c.351-236T>C	XP_011527315.1:n.351-236T>C
XM_011529014.1:c.351-236T>C	XP_011527316.1:n.351-236T>C
XM_011529013.2:c.351-236T>C	XP_011527315.1:n.351-236T>C
XM_017028024.1:c.369-236T>C	XP_016883513.1:n.369-236T>C
XM_017028025.1:c.369-236T>C	XP_016883514.1:n.369-236T>C
XM_017028026.1:c.369-236T>C	XP_016883515.1:n.369-236T>C
XM_017028027.2:c.369-236T>C	XP_016883516.1:n.369-236T>C
NM_005417.5:c.351-236T>C	NP_005408.1:n.351-236T>C
NM_198291.3:c.351-236T>C MANE Select	NP_938033.1:n.351-236T>C