Canonical Allele Identifier: CA2015327558

Gene: A2M KLRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9068574A= , CM000674.2:g.9068574A=	GRCh38
NC_000012.11:g.9221170A= , CM000674.1:g.9221170A=	GRCh37
NC_000012.10:g.9112437A=	NCBI36
NG_011717.1:g.52389T=
NG_011717.2:g.52389T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000318602.12:c.4366+166T= (A2M) MANE Select	ENSP00000323929.8:n.4366+166T=
ENST00000318602.11:c.4366+166T= (A2M)	ENSP00000323929.7:n.4366+166T=
ENST00000495442.1:n.216+166T= (A2M)
ENST00000495709.1:n.339+166T= (A2M)
ENST00000543436.2:n.452-762T= (A2M)
NM_000014.4:c.4366+166T= (A2M)	NP_000005.2:n.4366+166T=
XM_006719056.2:c.4366+166T= (A2M)	XP_006719119.1:n.4366+166T=
NM_000014.5:c.4366+166T= (A2M)	NP_000005.2:n.4366+166T=
NM_001347423.1:c.4366+166T= (A2M)	NP_001334352.1:n.4366+166T=
NM_001347424.1:c.4066+166T= (A2M)	NP_001334353.1:n.4066+166T=
NM_001347425.1:c.3916+166T= (A2M)	NP_001334354.1:n.3916+166T=
XM_006719056.3:c.4366+166T= (A2M)	XP_006719119.1:n.4366+166T=
XM_017018683.1:c.*33+10408A= (KLRG1)	XP_016874172.1:n.*33+10408A=
XM_017018684.1:c.*33+10408A= (KLRG1)	XP_016874173.1:n.*33+10408A=
XM_017018685.1:c.*33+10408A= (KLRG1)	XP_016874174.1:n.*33+10408A=
NM_000014.6:c.4366+166T= (A2M) MANE Select	NP_000005.3:n.4366+166T=
NM_001347423.2:c.4366+166T= (A2M)	NP_001334352.2:n.4366+166T=
NM_001347424.2:c.4066+166T= (A2M)	NP_001334353.2:n.4066+166T=
NM_001347425.2:c.3916+166T= (A2M)	NP_001334354.2:n.3916+166T=