Canonical Allele Identifier: CA2617528304

Gene: A2M KLRG1

Linked Data

• gnomAD v4: 12-9068630-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9068630A>G , CM000674.2:g.9068630A>G	GRCh38
NC_000012.11:g.9221226A>G , CM000674.1:g.9221226A>G	GRCh37
NC_000012.10:g.9112493A>G	NCBI36
NG_011717.1:g.52333T>C
NG_011717.2:g.52333T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000318602.12:c.4366+110T>C (A2M) MANE Select	ENSP00000323929.8:n.4366+110T>C
ENST00000318602.11:c.4366+110T>C (A2M)	ENSP00000323929.7:n.4366+110T>C
ENST00000495442.1:n.216+110T>C (A2M)
ENST00000495709.1:n.339+110T>C (A2M)
ENST00000543436.2:n.452-818T>C (A2M)
NM_000014.4:c.4366+110T>C (A2M)	NP_000005.2:n.4366+110T>C
XM_006719056.2:c.4366+110T>C (A2M)	XP_006719119.1:n.4366+110T>C
NM_000014.5:c.4366+110T>C (A2M)	NP_000005.2:n.4366+110T>C
NM_001347423.1:c.4366+110T>C (A2M)	NP_001334352.1:n.4366+110T>C
NM_001347424.1:c.4066+110T>C (A2M)	NP_001334353.1:n.4066+110T>C
NM_001347425.1:c.3916+110T>C (A2M)	NP_001334354.1:n.3916+110T>C
XM_006719056.3:c.4366+110T>C (A2M)	XP_006719119.1:n.4366+110T>C
XM_017018683.1:c.*33+10464A>G (KLRG1)	XP_016874172.1:n.*33+10464A>G
XM_017018684.1:c.*33+10464A>G (KLRG1)	XP_016874173.1:n.*33+10464A>G
XM_017018685.1:c.*33+10464A>G (KLRG1)	XP_016874174.1:n.*33+10464A>G
NM_000014.6:c.4366+110T>C (A2M) MANE Select	NP_000005.3:n.4366+110T>C
NM_001347423.2:c.4366+110T>C (A2M)	NP_001334352.2:n.4366+110T>C
NM_001347424.2:c.4066+110T>C (A2M)	NP_001334353.2:n.4066+110T>C
NM_001347425.2:c.3916+110T>C (A2M)	NP_001334354.2:n.3916+110T>C