Canonical Allele Identifier: CA2015346955

Gene: A2M KLRG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9115826A= , CM000674.2:g.9115826A=	GRCh38
NC_000012.11:g.9268422A= , CM000674.1:g.9268422A=	GRCh37
NC_000012.10:g.9159689A=	NCBI36
NG_011717.1:g.5137T=
NG_011717.2:g.5137T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.12:c.24T= (A2M) MANE Select	ENSP00000323929.8:p.His8=
ENST00000318602.11:c.24T= (A2M)	ENSP00000323929.7:p.His8=
ENST00000404455.2:c.24T= (A2M)	ENSP00000385710.2:p.His8=
ENST00000467091.1:n.236T= (A2M)
ENST00000497324.1:n.192T= (A2M)
ENST00000539638.5:c.24T= (A2M)	ENSP00000445717.1:p.His8=
NM_000014.4:c.24T= (A2M)	NP_000005.2:p.His8=
XM_006719056.2:c.24T= (A2M)	XP_006719119.1:p.His8=
NM_000014.5:c.24T= (A2M)	NP_000005.2:p.His8=
NM_001347423.1:c.24T= (A2M)	NP_001334352.1:p.His8=
NM_001347424.1:c.-430T= (A2M)	NP_001334353.1:n.-430T=
NM_001347425.1:c.-267T= (A2M)	NP_001334354.1:n.-267T=
XM_006719056.3:c.24T= (A2M)	XP_006719119.1:p.His8=
XM_017018683.1:c.*34-9548A= (KLRG1)	XP_016874172.1:n.*34-9548A=
XM_017018684.1:c.*34-19260A= (KLRG1)	XP_016874173.1:n.*34-19260A=
XM_017018685.1:c.*33+57660A= (KLRG1)	XP_016874174.1:n.*33+57660A=
NM_000014.6:c.24T= (A2M) MANE Select	NP_000005.3:p.His8=
NM_001347423.2:c.24T= (A2M)	NP_001334352.2:p.His8=
NM_001347424.2:c.-430T= (A2M)	NP_001334353.2:n.-430T=
NM_001347425.2:c.-267T= (A2M)	NP_001334354.2:n.-267T=