Canonical Allele Identifier: CA478327455

Gene: A2M KLRG1

Linked Data

• MyVariant Identifiers: chr12:g.9242543A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9089947A>C , CM000674.2:g.9089947A>C	GRCh38
NC_000012.11:g.9242543A>C , CM000674.1:g.9242543A>C	GRCh37
NC_000012.10:g.9133810A>C	NCBI36
NG_011717.1:g.31016T>G
NG_011717.2:g.31016T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.12:c.2673T>G (A2M) MANE Select	ENSP00000323929.8:p.Pro891=
ENST00000318602.11:c.2673T>G (A2M)	ENSP00000323929.7:p.Pro891=
ENST00000462568.1:n.252T>G (A2M)
ENST00000543436.2:n.416T>G (A2M)
ENST00000545828.1:n.348+11603T>G (A2M)
NM_000014.4:c.2673T>G (A2M)	NP_000005.2:p.Pro891=
XM_006719056.2:c.2673T>G (A2M)	XP_006719119.1:p.Pro891=
NM_000014.5:c.2673T>G (A2M)	NP_000005.2:p.Pro891=
NM_001347423.1:c.2673T>G (A2M)	NP_001334352.1:p.Pro891=
NM_001347424.1:c.2373T>G (A2M)	NP_001334353.1:p.Pro791=
NM_001347425.1:c.2223T>G (A2M)	NP_001334354.1:p.Pro741=
XM_006719056.3:c.2673T>G (A2M)	XP_006719119.1:p.Pro891=
XM_017018683.1:c.*33+31781A>C (KLRG1)	XP_016874172.1:n.*33+31781A>C
XM_017018684.1:c.*33+31781A>C (KLRG1)	XP_016874173.1:n.*33+31781A>C
XM_017018685.1:c.*33+31781A>C (KLRG1)	XP_016874174.1:n.*33+31781A>C
NM_000014.6:c.2673T>G (A2M) MANE Select	NP_000005.3:p.Pro891=
NM_001347423.2:c.2673T>G (A2M)	NP_001334352.2:p.Pro891=
NM_001347424.2:c.2373T>G (A2M)	NP_001334353.2:p.Pro791=
NM_001347425.2:c.2223T>G (A2M)	NP_001334354.2:p.Pro741=