Canonical Allele Identifier: CA2739428664

Gene: A2M KLRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9115885T>A , CM000674.2:g.9115885T>A	GRCh38
NC_000012.11:g.9268481T>A , CM000674.1:g.9268481T>A	GRCh37
NC_000012.10:g.9159748T>A	NCBI36
NG_011717.1:g.5078A>T
NG_011717.2:g.5078A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.12:c.-36A>T (A2M) MANE Select	ENSP00000323929.8:n.-36A>T
ENST00000318602.11:c.-36A>T (A2M)	ENSP00000323929.7:n.-36A>T
ENST00000404455.2:c.-17-19A>T (A2M)	ENSP00000385710.2:n.-17-19A>T
ENST00000467091.1:n.177A>T (A2M)
ENST00000497324.1:n.133A>T (A2M)
NM_000014.4:c.-36A>T (A2M)	NP_000005.2:n.-36A>T
XM_006719056.2:c.-36A>T (A2M)	XP_006719119.1:n.-36A>T
NM_000014.5:c.-36A>T (A2M)	NP_000005.2:n.-36A>T
NM_001347423.1:c.-17-19A>T (A2M)	NP_001334352.1:n.-17-19A>T
NM_001347424.1:c.-489A>T (A2M)	NP_001334353.1:n.-489A>T
NM_001347425.1:c.-326A>T (A2M)	NP_001334354.1:n.-326A>T
XM_006719056.3:c.-36A>T (A2M)	XP_006719119.1:n.-36A>T
XM_017018683.1:c.*34-9489T>A (KLRG1)	XP_016874172.1:n.*34-9489T>A
XM_017018684.1:c.*34-19201T>A (KLRG1)	XP_016874173.1:n.*34-19201T>A
XM_017018685.1:c.*33+57719T>A (KLRG1)	XP_016874174.1:n.*33+57719T>A
NM_000014.6:c.-36A>T (A2M) MANE Select	NP_000005.3:n.-36A>T
NM_001347423.2:c.-17-19A>T (A2M)	NP_001334352.2:n.-17-19A>T
NM_001347424.2:c.-489A>T (A2M)	NP_001334353.2:n.-489A>T
NM_001347425.2:c.-326A>T (A2M)	NP_001334354.2:n.-326A>T