Canonical Allele Identifier: CA2617534692

Gene: A2M KLRG1

Linked Data

• gnomAD v4: 12-9116032-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9116032C>A , CM000674.2:g.9116032C>A	GRCh38
NC_000012.11:g.9268628C>A , CM000674.1:g.9268628C>A	GRCh37
NC_000012.10:g.9159895C>A	NCBI36
NG_011717.1:g.4931G>T
NG_011717.2:g.4931G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318602.11:c.-183G>T (A2M)	ENSP00000323929.7:n.-183G>T
ENST00000404455.2:c.-18+96G>T (A2M)	ENSP00000385710.2:n.-18+96G>T
ENST00000467091.1:n.30G>T (A2M)
NM_000014.5:c.-183G>T (A2M)	NP_000005.2:n.-183G>T
NM_001347423.1:c.-18+96G>T (A2M)	NP_001334352.1:n.-18+96G>T
NM_001347424.1:c.-636G>T (A2M)	NP_001334353.1:n.-636G>T
NM_001347425.1:c.-473G>T (A2M)	NP_001334354.1:n.-473G>T
XM_017018683.1:c.*34-9342C>A (KLRG1)	XP_016874172.1:n.*34-9342C>A
XM_017018684.1:c.*34-19054C>A (KLRG1)	XP_016874173.1:n.*34-19054C>A
XM_017018685.1:c.*33+57866C>A (KLRG1)	XP_016874174.1:n.*33+57866C>A
NM_001347423.2:c.-18+96G>T (A2M)	NP_001334352.2:n.-18+96G>T