Canonical Allele Identifier: CA2015332132

Gene: A2M KLRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9079692G= , CM000674.2:g.9079692G=	GRCh38
NC_000012.11:g.9232288G= , CM000674.1:g.9232288G=	GRCh37
NC_000012.10:g.9123555G=	NCBI36
NG_011717.1:g.41271C=
NG_011717.2:g.41271C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.12:c.2978C= (A2M) MANE Select	ENSP00000323929.8:p.Thr993=
ENST00000318602.11:c.2978C= (A2M)	ENSP00000323929.7:p.Thr993=
ENST00000542567.1:n.333C= (A2M)
ENST00000543436.2:n.451+10220C= (A2M)
ENST00000545828.1:n.349-6971C= (A2M)
NM_000014.4:c.2978C= (A2M)	NP_000005.2:p.Thr993=
XM_006719056.2:c.2978C= (A2M)	XP_006719119.1:p.Thr993=
NM_000014.5:c.2978C= (A2M)	NP_000005.2:p.Thr993=
NM_001347423.1:c.2978C= (A2M)	NP_001334352.1:p.Thr993=
NM_001347424.1:c.2678C= (A2M)	NP_001334353.1:p.Thr893=
NM_001347425.1:c.2528C= (A2M)	NP_001334354.1:p.Thr843=
XM_006719056.3:c.2978C= (A2M)	XP_006719119.1:p.Thr993=
XM_017018683.1:c.*33+21526G= (KLRG1)	XP_016874172.1:n.*33+21526G=
XM_017018684.1:c.*33+21526G= (KLRG1)	XP_016874173.1:n.*33+21526G=
XM_017018685.1:c.*33+21526G= (KLRG1)	XP_016874174.1:n.*33+21526G=
NM_000014.6:c.2978C= (A2M) MANE Select	NP_000005.3:p.Thr993=
NM_001347423.2:c.2978C= (A2M)	NP_001334352.2:p.Thr993=
NM_001347424.2:c.2678C= (A2M)	NP_001334353.2:p.Thr893=
NM_001347425.2:c.2528C= (A2M)	NP_001334354.2:p.Thr843=