Canonical Allele Identifier: CA2657584597
Gene: CHKB HGNC NCBI
CHKB-CPT1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50582518_50582551dup , CM000684.2:g.50582518_50582551dup GRCh38
NC_000022.10:g.51020947_51020980dup , CM000684.1:g.51020947_51020980dup GRCh37
NC_000022.9:g.49367813_49367846dup NCBI36
NG_012643.1:g.1132_1165dup
NG_029213.1:g.5464_5497dup , LRG_855:g.5464_5497dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000406938.3:c.224+22_224+55dup (CHKB) MANE Select ENSP00000384400.3:n.224+22_224+55dup
ENST00000406938.2:c.224+22_224+55dup (CHKB) ENSP00000384400.2:n.224+22_224+55dup
ENST00000463053.1:n.307-179_307-146dup (CHKB)
ENST00000476289.5:n.319_352dup (CHKB)
ENST00000479003.5:n.285_318dup (CHKB)
ENST00000481673.5:n.288+22_288+55dup (CHKB)
ENST00000484266.5:n.289_322dup (CHKB)
ENST00000492556.5:n.430_463dup (CHKB-CPT1B)
ENST00000492582.5:n.319_352dup (CHKB)
NM_005198.4:c.224+22_224+55dup , LRG_855t1:c.224+22_224+55dup (CHKB) NP_005189.2:n.224+22_224+55dup
NR_027928.2:n.442+22_442+55dup (CHKB-CPT1B)
NM_005198.5:c.224+22_224+55dup (CHKB) MANE Select NP_005189.2:n.224+22_224+55dup