Canonical Allele Identifier: CA2739428643

Gene: A2M KLRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9115867C>A , CM000674.2:g.9115867C>A	GRCh38
NC_000012.11:g.9268463C>A , CM000674.1:g.9268463C>A	GRCh37
NC_000012.10:g.9159730C>A	NCBI36
NG_011717.1:g.5096G>T
NG_011717.2:g.5096G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.12:c.-18G>T (A2M) MANE Select	ENSP00000323929.8:n.-18G>T
ENST00000318602.11:c.-18G>T (A2M)	ENSP00000323929.7:n.-18G>T
ENST00000404455.2:c.-17-1G>T (A2M)	ENSP00000385710.2:n.-17-1G>T
ENST00000467091.1:n.195G>T (A2M)
ENST00000497324.1:n.151G>T (A2M)
NM_000014.4:c.-18G>T (A2M)	NP_000005.2:n.-18G>T
XM_006719056.2:c.-18G>T (A2M)	XP_006719119.1:n.-18G>T
NM_000014.5:c.-18G>T (A2M)	NP_000005.2:n.-18G>T
NM_001347423.1:c.-17-1G>T (A2M)	NP_001334352.1:n.-17-1G>T
NM_001347424.1:c.-471G>T (A2M)	NP_001334353.1:n.-471G>T
NM_001347425.1:c.-308G>T (A2M)	NP_001334354.1:n.-308G>T
XM_006719056.3:c.-18G>T (A2M)	XP_006719119.1:n.-18G>T
XM_017018683.1:c.*34-9507C>A (KLRG1)	XP_016874172.1:n.*34-9507C>A
XM_017018684.1:c.*34-19219C>A (KLRG1)	XP_016874173.1:n.*34-19219C>A
XM_017018685.1:c.*33+57701C>A (KLRG1)	XP_016874174.1:n.*33+57701C>A
NM_000014.6:c.-18G>T (A2M) MANE Select	NP_000005.3:n.-18G>T
NM_001347423.2:c.-17-1G>T (A2M)	NP_001334352.2:n.-17-1G>T
NM_001347424.2:c.-471G>T (A2M)	NP_001334353.2:n.-471G>T
NM_001347425.2:c.-308G>T (A2M)	NP_001334354.2:n.-308G>T