Canonical Allele Identifier: CA2015346996

Gene: A2M KLRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9115912C= , CM000674.2:g.9115912C=	GRCh38
NC_000012.11:g.9268508C= , CM000674.1:g.9268508C=	GRCh37
NC_000012.10:g.9159775C=	NCBI36
NG_011717.1:g.5051G=
NG_011717.2:g.5051G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000318602.12:c.-63G= (A2M) MANE Select	ENSP00000323929.8:n.-63G=
ENST00000318602.11:c.-63G= (A2M)	ENSP00000323929.7:n.-63G=
ENST00000404455.2:c.-17-46G= (A2M)	ENSP00000385710.2:n.-17-46G=
ENST00000467091.1:n.150G= (A2M)
ENST00000497324.1:n.106G= (A2M)
NM_000014.4:c.-63G= (A2M)	NP_000005.2:n.-63G=
XM_006719056.2:c.-63G= (A2M)	XP_006719119.1:n.-63G=
NM_000014.5:c.-63G= (A2M)	NP_000005.2:n.-63G=
NM_001347423.1:c.-17-46G= (A2M)	NP_001334352.1:n.-17-46G=
NM_001347424.1:c.-516G= (A2M)	NP_001334353.1:n.-516G=
NM_001347425.1:c.-353G= (A2M)	NP_001334354.1:n.-353G=
XM_006719056.3:c.-63G= (A2M)	XP_006719119.1:n.-63G=
XM_017018683.1:c.*34-9462C= (KLRG1)	XP_016874172.1:n.*34-9462C=
XM_017018684.1:c.*34-19174C= (KLRG1)	XP_016874173.1:n.*34-19174C=
XM_017018685.1:c.*33+57746C= (KLRG1)	XP_016874174.1:n.*33+57746C=
NM_000014.6:c.-63G= (A2M) MANE Select	NP_000005.3:n.-63G=
NM_001347423.2:c.-17-46G= (A2M)	NP_001334352.2:n.-17-46G=
NM_001347424.2:c.-516G= (A2M)	NP_001334353.2:n.-516G=
NM_001347425.2:c.-353G= (A2M)	NP_001334354.2:n.-353G=