Canonical Allele Identifier: CA2015332083

Gene: A2M KLRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9079590T= , CM000674.2:g.9079590T=	GRCh38
NC_000012.11:g.9232186T= , CM000674.1:g.9232186T=	GRCh37
NC_000012.10:g.9123453T=	NCBI36
NG_011717.1:g.41373A=
NG_011717.2:g.41373A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000318602.12:c.3031+49A= (A2M) MANE Select	ENSP00000323929.8:n.3031+49A=
ENST00000318602.11:c.3031+49A= (A2M)	ENSP00000323929.7:n.3031+49A=
ENST00000542567.1:n.386+49A= (A2M)
ENST00000543436.2:n.451+10322A= (A2M)
ENST00000545828.1:n.349-6869A= (A2M)
NM_000014.4:c.3031+49A= (A2M)	NP_000005.2:n.3031+49A=
XM_006719056.2:c.3031+49A= (A2M)	XP_006719119.1:n.3031+49A=
NM_000014.5:c.3031+49A= (A2M)	NP_000005.2:n.3031+49A=
NM_001347423.1:c.3031+49A= (A2M)	NP_001334352.1:n.3031+49A=
NM_001347424.1:c.2731+49A= (A2M)	NP_001334353.1:n.2731+49A=
NM_001347425.1:c.2581+49A= (A2M)	NP_001334354.1:n.2581+49A=
XM_006719056.3:c.3031+49A= (A2M)	XP_006719119.1:n.3031+49A=
XM_017018683.1:c.*33+21424T= (KLRG1)	XP_016874172.1:n.*33+21424T=
XM_017018684.1:c.*33+21424T= (KLRG1)	XP_016874173.1:n.*33+21424T=
XM_017018685.1:c.*33+21424T= (KLRG1)	XP_016874174.1:n.*33+21424T=
NM_000014.6:c.3031+49A= (A2M) MANE Select	NP_000005.3:n.3031+49A=
NM_001347423.2:c.3031+49A= (A2M)	NP_001334352.2:n.3031+49A=
NM_001347424.2:c.2731+49A= (A2M)	NP_001334353.2:n.2731+49A=
NM_001347425.2:c.2581+49A= (A2M)	NP_001334354.2:n.2581+49A=