Canonical Allele Identifier: CA2657584047

Gene: CHKB CHKB-CPT1B

Linked Data

• gnomAD v4: 22-50582047-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50582048del , CM000684.2:g.50582048del	GRCh38
NC_000022.10:g.51020477del , CM000684.1:g.51020477del	GRCh37
NC_000022.9:g.49367343del	NCBI36
NG_012643.1:g.1620del
NG_029213.1:g.5952del , LRG_855:g.5952del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406938.3:c.334-186del (CHKB) MANE Select	ENSP00000384400.3:n.334-186del
ENST00000406938.2:c.334-186del (CHKB)	ENSP00000384400.2:n.334-186del
ENST00000463053.1:n.463del (CHKB)
ENST00000465842.1:n.173-186del (CHKB)
ENST00000468532.5:n.211-186del (CHKB)
ENST00000476289.5:n.607-186del (CHKB)
ENST00000479003.5:n.773del (CHKB)
ENST00000481673.5:n.598del (CHKB)
ENST00000484266.5:n.576+201del (CHKB)
ENST00000492556.5:n.918del (CHKB-CPT1B)
ENST00000492582.5:n.807del (CHKB)
NM_005198.4:c.334-186del , LRG_855t1:c.334-186del (CHKB)	NP_005189.2:n.334-186del
NR_027928.2:n.552-186del (CHKB-CPT1B)
NM_005198.5:c.334-186del (CHKB) MANE Select	NP_005189.2:n.334-186del