Canonical Allele Identifier: CA2617528434

Gene: A2M KLRG1

Linked Data

• gnomAD v4: 12-9068912-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9068912T>A , CM000674.2:g.9068912T>A	GRCh38
NC_000012.11:g.9221508T>A , CM000674.1:g.9221508T>A	GRCh37
NC_000012.10:g.9112775T>A	NCBI36
NG_011717.1:g.52051A>T
NG_011717.2:g.52051A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.12:c.4264-70A>T (A2M) MANE Select	ENSP00000323929.8:n.4264-70A>T
ENST00000318602.11:c.4264-70A>T (A2M)	ENSP00000323929.7:n.4264-70A>T
ENST00000495442.1:n.44A>T (A2M)
ENST00000495709.1:n.167A>T (A2M)
ENST00000543436.2:n.452-1100A>T (A2M)
NM_000014.4:c.4264-70A>T (A2M)	NP_000005.2:n.4264-70A>T
XM_006719056.2:c.4264-70A>T (A2M)	XP_006719119.1:n.4264-70A>T
NM_000014.5:c.4264-70A>T (A2M)	NP_000005.2:n.4264-70A>T
NM_001347423.1:c.4264-70A>T (A2M)	NP_001334352.1:n.4264-70A>T
NM_001347424.1:c.3964-70A>T (A2M)	NP_001334353.1:n.3964-70A>T
NM_001347425.1:c.3814-70A>T (A2M)	NP_001334354.1:n.3814-70A>T
XM_006719056.3:c.4264-70A>T (A2M)	XP_006719119.1:n.4264-70A>T
XM_017018683.1:c.*33+10746T>A (KLRG1)	XP_016874172.1:n.*33+10746T>A
XM_017018684.1:c.*33+10746T>A (KLRG1)	XP_016874173.1:n.*33+10746T>A
XM_017018685.1:c.*33+10746T>A (KLRG1)	XP_016874174.1:n.*33+10746T>A
NM_000014.6:c.4264-70A>T (A2M) MANE Select	NP_000005.3:n.4264-70A>T
NM_001347423.2:c.4264-70A>T (A2M)	NP_001334352.2:n.4264-70A>T
NM_001347424.2:c.3964-70A>T (A2M)	NP_001334353.2:n.3964-70A>T
NM_001347425.2:c.3814-70A>T (A2M)	NP_001334354.2:n.3814-70A>T