Canonical Allele Identifier: CA383839059

Gene: A2M KLRG1

Linked Data

• MyVariant Identifiers: chr12:g.9232234C>G (hg19) ; chr12:g.9079638C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9079638C>G , CM000674.2:g.9079638C>G	GRCh38
NC_000012.11:g.9232234C>G , CM000674.1:g.9232234C>G	GRCh37
NC_000012.10:g.9123501C>G	NCBI36
NG_011717.1:g.41325G>C
NG_011717.2:g.41325G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.12:c.3031+1G>C (A2M) MANE Select	ENSP00000323929.8:n.3031+1G>C
ENST00000318602.11:c.3031+1G>C (A2M)	ENSP00000323929.7:n.3031+1G>C
ENST00000542567.1:n.386+1G>C (A2M)
ENST00000543436.2:n.451+10274G>C (A2M)
ENST00000545828.1:n.349-6917G>C (A2M)
NM_000014.4:c.3031+1G>C (A2M)	NP_000005.2:n.3031+1G>C
XM_006719056.2:c.3031+1G>C (A2M)	XP_006719119.1:n.3031+1G>C
NM_000014.5:c.3031+1G>C (A2M)	NP_000005.2:n.3031+1G>C
NM_001347423.1:c.3031+1G>C (A2M)	NP_001334352.1:n.3031+1G>C
NM_001347424.1:c.2731+1G>C (A2M)	NP_001334353.1:n.2731+1G>C
NM_001347425.1:c.2581+1G>C (A2M)	NP_001334354.1:n.2581+1G>C
XM_006719056.3:c.3031+1G>C (A2M)	XP_006719119.1:n.3031+1G>C
XM_017018683.1:c.*33+21472C>G (KLRG1)	XP_016874172.1:n.*33+21472C>G
XM_017018684.1:c.*33+21472C>G (KLRG1)	XP_016874173.1:n.*33+21472C>G
XM_017018685.1:c.*33+21472C>G (KLRG1)	XP_016874174.1:n.*33+21472C>G
NM_000014.6:c.3031+1G>C (A2M) MANE Select	NP_000005.3:n.3031+1G>C
NM_001347423.2:c.3031+1G>C (A2M)	NP_001334352.2:n.3031+1G>C
NM_001347424.2:c.2731+1G>C (A2M)	NP_001334353.2:n.2731+1G>C
NM_001347425.2:c.2581+1G>C (A2M)	NP_001334354.2:n.2581+1G>C