Canonical Allele Identifier: CA2015347004

Gene: A2M KLRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9115921A= , CM000674.2:g.9115921A=	GRCh38
NC_000012.11:g.9268517A= , CM000674.1:g.9268517A=	GRCh37
NC_000012.10:g.9159784A=	NCBI36
NG_011717.1:g.5042T=
NG_011717.2:g.5042T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.11:c.-72T= (A2M)	ENSP00000323929.7:n.-72T=
ENST00000404455.2:c.-17-55T= (A2M)	ENSP00000385710.2:n.-17-55T=
ENST00000467091.1:n.141T= (A2M)
ENST00000497324.1:n.97T= (A2M)
NM_000014.4:c.-72T= (A2M)	NP_000005.2:n.-72T=
XM_006719056.2:c.-72T= (A2M)	XP_006719119.1:n.-72T=
NM_000014.5:c.-72T= (A2M)	NP_000005.2:n.-72T=
NM_001347423.1:c.-17-55T= (A2M)	NP_001334352.1:n.-17-55T=
NM_001347424.1:c.-525T= (A2M)	NP_001334353.1:n.-525T=
NM_001347425.1:c.-362T= (A2M)	NP_001334354.1:n.-362T=
XM_006719056.3:c.-72T= (A2M)	XP_006719119.1:n.-72T=
XM_017018683.1:c.*34-9453A= (KLRG1)	XP_016874172.1:n.*34-9453A=
XM_017018684.1:c.*34-19165A= (KLRG1)	XP_016874173.1:n.*34-19165A=
XM_017018685.1:c.*33+57755A= (KLRG1)	XP_016874174.1:n.*33+57755A=
NM_001347423.2:c.-17-55T= (A2M)	NP_001334352.2:n.-17-55T=