Canonical Allele Identifier: CA127863

Gene: A2M KLRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9094987C>T , CM000674.2:g.9094987C>T	GRCh38
NC_000012.11:g.9247583C>T , CM000674.1:g.9247583C>T	GRCh37
NC_000012.10:g.9138850C>T	NCBI36
NG_011717.1:g.25976G>A
NG_011717.2:g.25976G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000014.6:c.2111G>A (A2M) MANE Select	NP_000005.3:p.Arg704His
ENST00000318602.12:c.2111G>A (A2M) MANE Select	ENSP00000323929.8:p.Arg704His
NM_000014.4:c.2111G>A (A2M)	NP_000005.2:p.Arg704His
NM_000014.5:c.2111G>A (A2M)	NP_000005.2:p.Arg704His
NM_001347423.1:c.2111G>A (A2M)	NP_001334352.1:p.Arg704His
NM_001347423.2:c.2111G>A (A2M)	NP_001334352.2:p.Arg704His
NM_001347424.1:c.1811G>A (A2M)	NP_001334353.1:p.Arg604His
NM_001347424.2:c.1811G>A (A2M)	NP_001334353.2:p.Arg604His
NM_001347425.1:c.1661G>A (A2M)	NP_001334354.1:p.Arg554His
NM_001347425.2:c.1661G>A (A2M)	NP_001334354.2:p.Arg554His
ENST00000318602.11:c.2111G>A (A2M)	ENSP00000323929.7:p.Arg704His
ENST00000545828.1:n.348+6563G>A (A2M)
ENST00000546069.1:c.430G>A (A2M)	ENSP00000438599.1:n.430G>A
XM_006719056.2:c.2111G>A (A2M)	XP_006719119.1:p.Arg704His
XM_006719056.3:c.2111G>A (A2M)	XP_006719119.1:p.Arg704His
XM_017018683.1:c.*34-30387C>T (KLRG1)	XP_016874172.1:n.*34-30387C>T
XM_017018684.1:c.*33+36821C>T (KLRG1)	XP_016874173.1:n.*33+36821C>T
XM_017018685.1:c.*33+36821C>T (KLRG1)	XP_016874174.1:n.*33+36821C>T