Canonical Allele Identifier: CA478343008

Gene: A2M KLRG1

Linked Data

• MyVariant Identifiers: chr12:g.9268410A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9115814A>C , CM000674.2:g.9115814A>C	GRCh38
NC_000012.11:g.9268410A>C , CM000674.1:g.9268410A>C	GRCh37
NC_000012.10:g.9159677A>C	NCBI36
NG_011717.1:g.5149T>G
NG_011717.2:g.5149T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.12:c.36T>G (A2M) MANE Select	ENSP00000323929.8:p.Val12=
ENST00000318602.11:c.36T>G (A2M)	ENSP00000323929.7:p.Val12=
ENST00000404455.2:c.36T>G (A2M)	ENSP00000385710.2:p.Val12=
ENST00000467091.1:n.248T>G (A2M)
ENST00000497324.1:n.204T>G (A2M)
ENST00000539638.5:c.36T>G (A2M)	ENSP00000445717.1:p.Val12=
NM_000014.4:c.36T>G (A2M)	NP_000005.2:p.Val12=
XM_006719056.2:c.36T>G (A2M)	XP_006719119.1:p.Val12=
NM_000014.5:c.36T>G (A2M)	NP_000005.2:p.Val12=
NM_001347423.1:c.36T>G (A2M)	NP_001334352.1:p.Val12=
NM_001347424.1:c.-418T>G (A2M)	NP_001334353.1:n.-418T>G
NM_001347425.1:c.-255T>G (A2M)	NP_001334354.1:n.-255T>G
XM_006719056.3:c.36T>G (A2M)	XP_006719119.1:p.Val12=
XM_017018683.1:c.*34-9560A>C (KLRG1)	XP_016874172.1:n.*34-9560A>C
XM_017018684.1:c.*34-19272A>C (KLRG1)	XP_016874173.1:n.*34-19272A>C
XM_017018685.1:c.*33+57648A>C (KLRG1)	XP_016874174.1:n.*33+57648A>C
NM_000014.6:c.36T>G (A2M) MANE Select	NP_000005.3:p.Val12=
NM_001347423.2:c.36T>G (A2M)	NP_001334352.2:p.Val12=
NM_001347424.2:c.-418T>G (A2M)	NP_001334353.2:n.-418T>G
NM_001347425.2:c.-255T>G (A2M)	NP_001334354.2:n.-255T>G