Canonical Allele Identifier: CA2657584042

Gene: CHKB CHKB-CPT1B

Linked Data

• gnomAD v4: 22-50582043-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50582045del , CM000684.2:g.50582045del	GRCh38
NC_000022.10:g.51020474del , CM000684.1:g.51020474del	GRCh37
NC_000022.9:g.49367340del	NCBI36
NG_012643.1:g.1624del
NG_029213.1:g.5956del , LRG_855:g.5956del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406938.3:c.334-182del (CHKB) MANE Select	ENSP00000384400.3:n.334-182del
ENST00000406938.2:c.334-182del (CHKB)	ENSP00000384400.2:n.334-182del
ENST00000463053.1:n.467del (CHKB)
ENST00000465842.1:n.173-182del (CHKB)
ENST00000468532.5:n.211-182del (CHKB)
ENST00000476289.5:n.607-182del (CHKB)
ENST00000479003.5:n.777del (CHKB)
ENST00000481673.5:n.602del (CHKB)
ENST00000484266.5:n.576+205del (CHKB)
ENST00000492556.5:n.922del (CHKB-CPT1B)
ENST00000492582.5:n.811del (CHKB)
NM_005198.4:c.334-182del , LRG_855t1:c.334-182del (CHKB)	NP_005189.2:n.334-182del
NR_027928.2:n.552-182del (CHKB-CPT1B)
NM_005198.5:c.334-182del (CHKB) MANE Select	NP_005189.2:n.334-182del