Canonical Allele Identifier: CA383828683

Gene: A2M KLRG1

Linked Data

• MyVariant Identifiers: chr12:g.9221356A>C (hg19) ; chr12:g.9068760A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9068760A>C , CM000674.2:g.9068760A>C	GRCh38
NC_000012.11:g.9221356A>C , CM000674.1:g.9221356A>C	GRCh37
NC_000012.10:g.9112623A>C	NCBI36
NG_011717.1:g.52203T>G
NG_011717.2:g.52203T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.12:c.4346T>G (A2M) MANE Select	ENSP00000323929.8:p.Val1449Gly
ENST00000318602.11:c.4346T>G (A2M)	ENSP00000323929.7:p.Val1449Gly
ENST00000495442.1:n.196T>G (A2M)
ENST00000495709.1:n.319T>G (A2M)
ENST00000543436.2:n.452-948T>G (A2M)
NM_000014.4:c.4346T>G (A2M)	NP_000005.2:p.Val1449Gly
XM_006719056.2:c.4346T>G (A2M)	XP_006719119.1:p.Val1449Gly
NM_000014.5:c.4346T>G (A2M)	NP_000005.2:p.Val1449Gly
NM_001347423.1:c.4346T>G (A2M)	NP_001334352.1:p.Val1449Gly
NM_001347424.1:c.4046T>G (A2M)	NP_001334353.1:p.Val1349Gly
NM_001347425.1:c.3896T>G (A2M)	NP_001334354.1:p.Val1299Gly
XM_006719056.3:c.4346T>G (A2M)	XP_006719119.1:p.Val1449Gly
XM_017018683.1:c.*33+10594A>C (KLRG1)	XP_016874172.1:n.*33+10594A>C
XM_017018684.1:c.*33+10594A>C (KLRG1)	XP_016874173.1:n.*33+10594A>C
XM_017018685.1:c.*33+10594A>C (KLRG1)	XP_016874174.1:n.*33+10594A>C
NM_000014.6:c.4346T>G (A2M) MANE Select	NP_000005.3:p.Val1449Gly
NM_001347423.2:c.4346T>G (A2M)	NP_001334352.2:p.Val1449Gly
NM_001347424.2:c.4046T>G (A2M)	NP_001334353.2:p.Val1349Gly
NM_001347425.2:c.3896T>G (A2M)	NP_001334354.2:p.Val1299Gly