Canonical Allele Identifier: CA603491129

Gene: A2M KLRG1

Linked Data

• dbSNP Id: rs1457700218
• gnomAD v2: 12-9232190-G-T
• gnomAD v4: 12-9079594-G-T
• MyVariant Identifiers: chr12:g.9232190G>T (hg19) ; chr12:g.9079594G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9079594G>T , CM000674.2:g.9079594G>T	GRCh38
NC_000012.11:g.9232190G>T , CM000674.1:g.9232190G>T	GRCh37
NC_000012.10:g.9123457G>T	NCBI36
NG_011717.1:g.41369C>A
NG_011717.2:g.41369C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000318602.12:c.3031+45C>A (A2M) MANE Select	ENSP00000323929.8:n.3031+45C>A
ENST00000318602.11:c.3031+45C>A (A2M)	ENSP00000323929.7:n.3031+45C>A
ENST00000542567.1:n.386+45C>A (A2M)
ENST00000543436.2:n.451+10318C>A (A2M)
ENST00000545828.1:n.349-6873C>A (A2M)
NM_000014.4:c.3031+45C>A (A2M)	NP_000005.2:n.3031+45C>A
XM_006719056.2:c.3031+45C>A (A2M)	XP_006719119.1:n.3031+45C>A
NM_000014.5:c.3031+45C>A (A2M)	NP_000005.2:n.3031+45C>A
NM_001347423.1:c.3031+45C>A (A2M)	NP_001334352.1:n.3031+45C>A
NM_001347424.1:c.2731+45C>A (A2M)	NP_001334353.1:n.2731+45C>A
NM_001347425.1:c.2581+45C>A (A2M)	NP_001334354.1:n.2581+45C>A
XM_006719056.3:c.3031+45C>A (A2M)	XP_006719119.1:n.3031+45C>A
XM_017018683.1:c.*33+21428G>T (KLRG1)	XP_016874172.1:n.*33+21428G>T
XM_017018684.1:c.*33+21428G>T (KLRG1)	XP_016874173.1:n.*33+21428G>T
XM_017018685.1:c.*33+21428G>T (KLRG1)	XP_016874174.1:n.*33+21428G>T
NM_000014.6:c.3031+45C>A (A2M) MANE Select	NP_000005.3:n.3031+45C>A
NM_001347423.2:c.3031+45C>A (A2M)	NP_001334352.2:n.3031+45C>A
NM_001347424.2:c.2731+45C>A (A2M)	NP_001334353.2:n.2731+45C>A
NM_001347425.2:c.2581+45C>A (A2M)	NP_001334354.2:n.2581+45C>A