Canonical Allele Identifier: CA412200981
Gene: CHKB HGNC NCBI
CHKB-CPT1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50581547G>A , CM000684.2:g.50581547G>A GRCh38
NC_000022.10:g.51019976G>A , CM000684.1:g.51019976G>A GRCh37
NC_000022.9:g.49366842G>A NCBI36
NG_012643.1:g.2121C>T
NG_029213.1:g.6453C>T , LRG_855:g.6453C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000406938.3:c.454C>T (CHKB) MANE Select ENSP00000384400.3:p.Pro152Ser
ENST00000406938.2:c.454C>T (CHKB) ENSP00000384400.2:p.Pro152Ser
ENST00000463053.1:n.603C>T (CHKB)
ENST00000468532.5:n.331C>T (CHKB)
ENST00000476289.5:n.727C>T (CHKB)
ENST00000479003.5:n.1079C>T (CHKB)
ENST00000481673.5:n.904C>T (CHKB)
ENST00000484266.5:n.576+702C>T (CHKB)
ENST00000492556.5:n.1224C>T (CHKB-CPT1B)
ENST00000492582.5:n.1113C>T (CHKB)
NM_005198.4:c.454C>T , LRG_855t1:c.454C>T (CHKB) NP_005189.2:p.Pro152Ser
NR_027928.2:n.672C>T (CHKB-CPT1B)
NM_005198.5:c.454C>T (CHKB) MANE Select NP_005189.2:p.Pro152Ser