Canonical Allele Identifier: CA2581069259

Gene: A2M KLRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9115989T>G , CM000674.2:g.9115989T>G	GRCh38
NC_000012.11:g.9268585T>G , CM000674.1:g.9268585T>G	GRCh37
NC_000012.10:g.9159852T>G	NCBI36
NG_011717.1:g.4974A>C
NG_011717.2:g.4974A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000318602.11:c.-140A>C (A2M)	ENSP00000323929.7:n.-140A>C
ENST00000404455.2:c.-17-123A>C (A2M)	ENSP00000385710.2:n.-17-123A>C
ENST00000467091.1:n.73A>C (A2M)
ENST00000497324.1:n.29A>C (A2M)
NM_000014.5:c.-140A>C (A2M)	NP_000005.2:n.-140A>C
NM_001347423.1:c.-17-123A>C (A2M)	NP_001334352.1:n.-17-123A>C
NM_001347424.1:c.-593A>C (A2M)	NP_001334353.1:n.-593A>C
NM_001347425.1:c.-430A>C (A2M)	NP_001334354.1:n.-430A>C
XM_017018683.1:c.*34-9385T>G (KLRG1)	XP_016874172.1:n.*34-9385T>G
XM_017018684.1:c.*34-19097T>G (KLRG1)	XP_016874173.1:n.*34-19097T>G
XM_017018685.1:c.*33+57823T>G (KLRG1)	XP_016874174.1:n.*33+57823T>G
NM_001347423.2:c.-17-123A>C (A2M)	NP_001334352.2:n.-17-123A>C