Canonical Allele Identifier: CA2739428668

Gene: A2M KLRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9115887T>G , CM000674.2:g.9115887T>G	GRCh38
NC_000012.11:g.9268483T>G , CM000674.1:g.9268483T>G	GRCh37
NC_000012.10:g.9159750T>G	NCBI36
NG_011717.1:g.5076A>C
NG_011717.2:g.5076A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.12:c.-38A>C (A2M) MANE Select	ENSP00000323929.8:n.-38A>C
ENST00000318602.11:c.-38A>C (A2M)	ENSP00000323929.7:n.-38A>C
ENST00000404455.2:c.-17-21A>C (A2M)	ENSP00000385710.2:n.-17-21A>C
ENST00000467091.1:n.175A>C (A2M)
ENST00000497324.1:n.131A>C (A2M)
NM_000014.4:c.-38A>C (A2M)	NP_000005.2:n.-38A>C
XM_006719056.2:c.-38A>C (A2M)	XP_006719119.1:n.-38A>C
NM_000014.5:c.-38A>C (A2M)	NP_000005.2:n.-38A>C
NM_001347423.1:c.-17-21A>C (A2M)	NP_001334352.1:n.-17-21A>C
NM_001347424.1:c.-491A>C (A2M)	NP_001334353.1:n.-491A>C
NM_001347425.1:c.-328A>C (A2M)	NP_001334354.1:n.-328A>C
XM_006719056.3:c.-38A>C (A2M)	XP_006719119.1:n.-38A>C
XM_017018683.1:c.*34-9487T>G (KLRG1)	XP_016874172.1:n.*34-9487T>G
XM_017018684.1:c.*34-19199T>G (KLRG1)	XP_016874173.1:n.*34-19199T>G
XM_017018685.1:c.*33+57721T>G (KLRG1)	XP_016874174.1:n.*33+57721T>G
NM_000014.6:c.-38A>C (A2M) MANE Select	NP_000005.3:n.-38A>C
NM_001347423.2:c.-17-21A>C (A2M)	NP_001334352.2:n.-17-21A>C
NM_001347424.2:c.-491A>C (A2M)	NP_001334353.2:n.-491A>C
NM_001347425.2:c.-328A>C (A2M)	NP_001334354.2:n.-328A>C