Canonical Allele Identifier: CA2617534645

Gene: A2M KLRG1

Linked Data

• gnomAD v4: 12-9115993-TAAAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9115997_9116000del , CM000674.2:g.9115997_9116000del	GRCh38
NC_000012.11:g.9268593_9268596del , CM000674.1:g.9268593_9268596del	GRCh37
NC_000012.10:g.9159860_9159863del	NCBI36
NG_011717.1:g.4966_4969del
NG_011717.2:g.4966_4969del

Transcript Alleles

HGVS	Amino-acid change
ENST00000318602.11:c.-148_-145del (A2M)	ENSP00000323929.7:n.-148_-145del
ENST00000404455.2:c.-17-131_-17-128del (A2M)	ENSP00000385710.2:n.-17-131_-17-128del
ENST00000467091.1:n.65_68del (A2M)
ENST00000497324.1:n.21_24del (A2M)
NM_000014.5:c.-148_-145del (A2M)	NP_000005.2:n.-148_-145del
NM_001347423.1:c.-17-131_-17-128del (A2M)	NP_001334352.1:n.-17-131_-17-128del
NM_001347424.1:c.-601_-598del (A2M)	NP_001334353.1:n.-601_-598del
NM_001347425.1:c.-438_-435del (A2M)	NP_001334354.1:n.-438_-435del
XM_017018683.1:c.*34-9377_*34-9374del (KLRG1)	XP_016874172.1:n.*34-9377_*34-9374del
XM_017018684.1:c.*34-19089_*34-19086del (KLRG1)	XP_016874173.1:n.*34-19089_*34-19086del
XM_017018685.1:c.*33+57831_*33+57834del (KLRG1)	XP_016874174.1:n.*33+57831_*33+57834del
NM_001347423.2:c.-17-131_-17-128del (A2M)	NP_001334352.2:n.-17-131_-17-128del