Canonical Allele Identifier: CA383844476

Gene: A2M KLRG1

Linked Data

• dbSNP Id: rs1949159249
• gnomAD v3: 12-9089961-C-T
• gnomAD v4: 12-9089961-C-T
• MyVariant Identifiers: chr12:g.9242557C>T (hg19) ; chr12:g.9089961C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9089961C>T , CM000674.2:g.9089961C>T	GRCh38
NC_000012.11:g.9242557C>T , CM000674.1:g.9242557C>T	GRCh37
NC_000012.10:g.9133824C>T	NCBI36
NG_011717.1:g.31002G>A
NG_011717.2:g.31002G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.12:c.2659G>A (A2M) MANE Select	ENSP00000323929.8:p.Val887Met
ENST00000318602.11:c.2659G>A (A2M)	ENSP00000323929.7:p.Val887Met
ENST00000462568.1:n.238G>A (A2M)
ENST00000543436.2:n.402G>A (A2M)
ENST00000545828.1:n.348+11589G>A (A2M)
NM_000014.4:c.2659G>A (A2M)	NP_000005.2:p.Val887Met
XM_006719056.2:c.2659G>A (A2M)	XP_006719119.1:p.Val887Met
NM_000014.5:c.2659G>A (A2M)	NP_000005.2:p.Val887Met
NM_001347423.1:c.2659G>A (A2M)	NP_001334352.1:p.Val887Met
NM_001347424.1:c.2359G>A (A2M)	NP_001334353.1:p.Val787Met
NM_001347425.1:c.2209G>A (A2M)	NP_001334354.1:p.Val737Met
XM_006719056.3:c.2659G>A (A2M)	XP_006719119.1:p.Val887Met
XM_017018683.1:c.*33+31795C>T (KLRG1)	XP_016874172.1:n.*33+31795C>T
XM_017018684.1:c.*33+31795C>T (KLRG1)	XP_016874173.1:n.*33+31795C>T
XM_017018685.1:c.*33+31795C>T (KLRG1)	XP_016874174.1:n.*33+31795C>T
NM_000014.6:c.2659G>A (A2M) MANE Select	NP_000005.3:p.Val887Met
NM_001347423.2:c.2659G>A (A2M)	NP_001334352.2:p.Val887Met
NM_001347424.2:c.2359G>A (A2M)	NP_001334353.2:p.Val787Met
NM_001347425.2:c.2209G>A (A2M)	NP_001334354.2:p.Val737Met