Canonical Allele Identifier: CA2739428676

Gene: A2M KLRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9115895T>A , CM000674.2:g.9115895T>A	GRCh38
NC_000012.11:g.9268491T>A , CM000674.1:g.9268491T>A	GRCh37
NC_000012.10:g.9159758T>A	NCBI36
NG_011717.1:g.5068A>T
NG_011717.2:g.5068A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000318602.12:c.-46A>T (A2M) MANE Select	ENSP00000323929.8:n.-46A>T
ENST00000318602.11:c.-46A>T (A2M)	ENSP00000323929.7:n.-46A>T
ENST00000404455.2:c.-17-29A>T (A2M)	ENSP00000385710.2:n.-17-29A>T
ENST00000467091.1:n.167A>T (A2M)
ENST00000497324.1:n.123A>T (A2M)
NM_000014.4:c.-46A>T (A2M)	NP_000005.2:n.-46A>T
XM_006719056.2:c.-46A>T (A2M)	XP_006719119.1:n.-46A>T
NM_000014.5:c.-46A>T (A2M)	NP_000005.2:n.-46A>T
NM_001347423.1:c.-17-29A>T (A2M)	NP_001334352.1:n.-17-29A>T
NM_001347424.1:c.-499A>T (A2M)	NP_001334353.1:n.-499A>T
NM_001347425.1:c.-336A>T (A2M)	NP_001334354.1:n.-336A>T
XM_006719056.3:c.-46A>T (A2M)	XP_006719119.1:n.-46A>T
XM_017018683.1:c.*34-9479T>A (KLRG1)	XP_016874172.1:n.*34-9479T>A
XM_017018684.1:c.*34-19191T>A (KLRG1)	XP_016874173.1:n.*34-19191T>A
XM_017018685.1:c.*33+57729T>A (KLRG1)	XP_016874174.1:n.*33+57729T>A
NM_000014.6:c.-46A>T (A2M) MANE Select	NP_000005.3:n.-46A>T
NM_001347423.2:c.-17-29A>T (A2M)	NP_001334352.2:n.-17-29A>T
NM_001347424.2:c.-499A>T (A2M)	NP_001334353.2:n.-499A>T
NM_001347425.2:c.-336A>T (A2M)	NP_001334354.2:n.-336A>T