Canonical Allele Identifier: CA2739428652

Gene: A2M KLRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9115875G>C , CM000674.2:g.9115875G>C	GRCh38
NC_000012.11:g.9268471G>C , CM000674.1:g.9268471G>C	GRCh37
NC_000012.10:g.9159738G>C	NCBI36
NG_011717.1:g.5088C>G
NG_011717.2:g.5088C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.12:c.-26C>G (A2M) MANE Select	ENSP00000323929.8:n.-26C>G
ENST00000318602.11:c.-26C>G (A2M)	ENSP00000323929.7:n.-26C>G
ENST00000404455.2:c.-17-9C>G (A2M)	ENSP00000385710.2:n.-17-9C>G
ENST00000467091.1:n.187C>G (A2M)
ENST00000497324.1:n.143C>G (A2M)
NM_000014.4:c.-26C>G (A2M)	NP_000005.2:n.-26C>G
XM_006719056.2:c.-26C>G (A2M)	XP_006719119.1:n.-26C>G
NM_000014.5:c.-26C>G (A2M)	NP_000005.2:n.-26C>G
NM_001347423.1:c.-17-9C>G (A2M)	NP_001334352.1:n.-17-9C>G
NM_001347424.1:c.-479C>G (A2M)	NP_001334353.1:n.-479C>G
NM_001347425.1:c.-316C>G (A2M)	NP_001334354.1:n.-316C>G
XM_006719056.3:c.-26C>G (A2M)	XP_006719119.1:n.-26C>G
XM_017018683.1:c.*34-9499G>C (KLRG1)	XP_016874172.1:n.*34-9499G>C
XM_017018684.1:c.*34-19211G>C (KLRG1)	XP_016874173.1:n.*34-19211G>C
XM_017018685.1:c.*33+57709G>C (KLRG1)	XP_016874174.1:n.*33+57709G>C
NM_000014.6:c.-26C>G (A2M) MANE Select	NP_000005.3:n.-26C>G
NM_001347423.2:c.-17-9C>G (A2M)	NP_001334352.2:n.-17-9C>G
NM_001347424.2:c.-479C>G (A2M)	NP_001334353.2:n.-479C>G
NM_001347425.2:c.-316C>G (A2M)	NP_001334354.2:n.-316C>G