Canonical Allele Identifier: CA2410936502
Gene: CHKB HGNC NCBI
CHKB-CPT1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50582531C= , CM000684.2:g.50582531C= GRCh38
NC_000022.10:g.51020960C= , CM000684.1:g.51020960C= GRCh37
NC_000022.9:g.49367826C= NCBI36
NG_012643.1:g.1137G=
NG_029213.1:g.5469G= , LRG_855:g.5469G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000406938.3:c.224+27G= (CHKB) MANE Select ENSP00000384400.3:n.224+27G=
ENST00000406938.2:c.224+27G= (CHKB) ENSP00000384400.2:n.224+27G=
ENST00000463053.1:n.307-174G= (CHKB)
ENST00000476289.5:n.324G= (CHKB)
ENST00000479003.5:n.290G= (CHKB)
ENST00000481673.5:n.288+27G= (CHKB)
ENST00000484266.5:n.294G= (CHKB)
ENST00000492556.5:n.435G= (CHKB-CPT1B)
ENST00000492582.5:n.324G= (CHKB)
NM_005198.4:c.224+27G= , LRG_855t1:c.224+27G= (CHKB) NP_005189.2:n.224+27G=
NR_027928.2:n.442+27G= (CHKB-CPT1B)
NM_005198.5:c.224+27G= (CHKB) MANE Select NP_005189.2:n.224+27G=