Canonical Allele Identifier: CA2617534932

Gene: A2M KLRG1

Linked Data

• gnomAD v4: 12-9116223-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9116224_9116225del , CM000674.2:g.9116224_9116225del	GRCh38
NC_000012.11:g.9268820_9268821del , CM000674.1:g.9268820_9268821del	GRCh37
NC_000012.10:g.9160087_9160088del	NCBI36
NG_011717.1:g.4738_4739del
NG_011717.2:g.4738_4739del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404455.2:c.-115_-114del (A2M)	ENSP00000385710.2:n.-115_-114del
NM_000014.5:c.-376_-375del (A2M)	NP_000005.2:n.-376_-375del
NM_001347423.1:c.-115_-114del (A2M)	NP_001334352.1:n.-115_-114del
NM_001347424.1:c.-829_-828del (A2M)	NP_001334353.1:n.-829_-828del
NM_001347425.1:c.-666_-665del (A2M)	NP_001334354.1:n.-666_-665del
XM_017018683.1:c.*34-9150_*34-9149del (KLRG1)	XP_016874172.1:n.*34-9150_*34-9149del
XM_017018684.1:c.*34-18862_*34-18861del (KLRG1)	XP_016874173.1:n.*34-18862_*34-18861del
XM_017018685.1:c.*33+58058_*33+58059del (KLRG1)	XP_016874174.1:n.*33+58058_*33+58059del
NM_001347423.2:c.-115_-114del (A2M)	NP_001334352.2:n.-115_-114del