Canonical Allele Identifier: CA2819320593
Gene: CHKB HGNC NCBI
CHKB-CPT1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50582519C>A , CM000684.2:g.50582519C>A GRCh38
NC_000022.10:g.51020948C>A , CM000684.1:g.51020948C>A GRCh37
NC_000022.9:g.49367814C>A NCBI36
NG_012643.1:g.1149G>T
NG_029213.1:g.5481G>T , LRG_855:g.5481G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000406938.3:c.224+39G>T (CHKB) MANE Select ENSP00000384400.3:n.224+39G>T
ENST00000406938.2:c.224+39G>T (CHKB) ENSP00000384400.2:n.224+39G>T
ENST00000463053.1:n.307-162G>T (CHKB)
ENST00000476289.5:n.336G>T (CHKB)
ENST00000479003.5:n.302G>T (CHKB)
ENST00000481673.5:n.288+39G>T (CHKB)
ENST00000484266.5:n.306G>T (CHKB)
ENST00000492556.5:n.447G>T (CHKB-CPT1B)
ENST00000492582.5:n.336G>T (CHKB)
NM_005198.4:c.224+39G>T , LRG_855t1:c.224+39G>T (CHKB) NP_005189.2:n.224+39G>T
NR_027928.2:n.442+39G>T (CHKB-CPT1B)
NM_005198.5:c.224+39G>T (CHKB) MANE Select NP_005189.2:n.224+39G>T