Canonical Allele Identifier: CA383855190

Gene: A2M KLRG1

Linked Data

• MyVariant Identifiers: chr12:g.9268435T>C (hg19) ; chr12:g.9115839T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9115839T>C , CM000674.2:g.9115839T>C	GRCh38
NC_000012.11:g.9268435T>C , CM000674.1:g.9268435T>C	GRCh37
NC_000012.10:g.9159702T>C	NCBI36
NG_011717.1:g.5124A>G
NG_011717.2:g.5124A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.12:c.11A>G (A2M) MANE Select	ENSP00000323929.8:p.Asn4Ser
ENST00000318602.11:c.11A>G (A2M)	ENSP00000323929.7:p.Asn4Ser
ENST00000404455.2:c.11A>G (A2M)	ENSP00000385710.2:p.Asn4Ser
ENST00000467091.1:n.223A>G (A2M)
ENST00000497324.1:n.179A>G (A2M)
ENST00000539638.5:c.11A>G (A2M)	ENSP00000445717.1:p.Asn4Ser
NM_000014.4:c.11A>G (A2M)	NP_000005.2:p.Asn4Ser
XM_006719056.2:c.11A>G (A2M)	XP_006719119.1:p.Asn4Ser
NM_000014.5:c.11A>G (A2M)	NP_000005.2:p.Asn4Ser
NM_001347423.1:c.11A>G (A2M)	NP_001334352.1:p.Asn4Ser
NM_001347424.1:c.-443A>G (A2M)	NP_001334353.1:n.-443A>G
NM_001347425.1:c.-280A>G (A2M)	NP_001334354.1:n.-280A>G
XM_006719056.3:c.11A>G (A2M)	XP_006719119.1:p.Asn4Ser
XM_017018683.1:c.*34-9535T>C (KLRG1)	XP_016874172.1:n.*34-9535T>C
XM_017018684.1:c.*34-19247T>C (KLRG1)	XP_016874173.1:n.*34-19247T>C
XM_017018685.1:c.*33+57673T>C (KLRG1)	XP_016874174.1:n.*33+57673T>C
NM_000014.6:c.11A>G (A2M) MANE Select	NP_000005.3:p.Asn4Ser
NM_001347423.2:c.11A>G (A2M)	NP_001334352.2:p.Asn4Ser
NM_001347424.2:c.-443A>G (A2M)	NP_001334353.2:n.-443A>G
NM_001347425.2:c.-280A>G (A2M)	NP_001334354.2:n.-280A>G