Canonical Allele Identifier: CA2015346969

Gene: A2M KLRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9115859A= , CM000674.2:g.9115859A=	GRCh38
NC_000012.11:g.9268455A= , CM000674.1:g.9268455A=	GRCh37
NC_000012.10:g.9159722A=	NCBI36
NG_011717.1:g.5104T=
NG_011717.2:g.5104T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.12:c.-10T= (A2M) MANE Select	ENSP00000323929.8:n.-10T=
ENST00000318602.11:c.-10T= (A2M)	ENSP00000323929.7:n.-10T=
ENST00000404455.2:c.-10T= (A2M)	ENSP00000385710.2:n.-10T=
ENST00000467091.1:n.203T= (A2M)
ENST00000497324.1:n.159T= (A2M)
ENST00000539638.5:c.-10T= (A2M)	ENSP00000445717.1:n.-10T=
NM_000014.4:c.-10T= (A2M)	NP_000005.2:n.-10T=
XM_006719056.2:c.-10T= (A2M)	XP_006719119.1:n.-10T=
NM_000014.5:c.-10T= (A2M)	NP_000005.2:n.-10T=
NM_001347423.1:c.-10T= (A2M)	NP_001334352.1:n.-10T=
NM_001347424.1:c.-463T= (A2M)	NP_001334353.1:n.-463T=
NM_001347425.1:c.-300T= (A2M)	NP_001334354.1:n.-300T=
XM_006719056.3:c.-10T= (A2M)	XP_006719119.1:n.-10T=
XM_017018683.1:c.*34-9515A= (KLRG1)	XP_016874172.1:n.*34-9515A=
XM_017018684.1:c.*34-19227A= (KLRG1)	XP_016874173.1:n.*34-19227A=
XM_017018685.1:c.*33+57693A= (KLRG1)	XP_016874174.1:n.*33+57693A=
NM_000014.6:c.-10T= (A2M) MANE Select	NP_000005.3:n.-10T=
NM_001347423.2:c.-10T= (A2M)	NP_001334352.2:n.-10T=
NM_001347424.2:c.-463T= (A2M)	NP_001334353.2:n.-463T=
NM_001347425.2:c.-300T= (A2M)	NP_001334354.2:n.-300T=