Canonical Allele Identifier: CA15999876

Gene: CHKB CHKB-CPT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50581640G>C , CM000684.2:g.50581640G>C	GRCh38
NC_000022.10:g.51020069G>C , CM000684.1:g.51020069G>C	GRCh37
NC_000022.9:g.49366935G>C	NCBI36
NG_012643.1:g.2028C>G
NG_029213.1:g.6360C>G , LRG_855:g.6360C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_005198.5:c.448-87C>G (CHKB) MANE Select	NP_005189.2:n.448-87C>G
ENST00000406938.3:c.448-87C>G (CHKB) MANE Select	ENSP00000384400.3:n.448-87C>G
NM_005198.4:c.448-87C>G , LRG_855t1:c.448-87C>G (CHKB)	NP_005189.2:n.448-87C>G
NR_027928.2:n.666-87C>G (CHKB-CPT1B)
ENST00000406938.2:c.448-87C>G (CHKB)	ENSP00000384400.2:n.448-87C>G
ENST00000463053.1:n.597-87C>G (CHKB)
ENST00000465842.1:n.395C>G (CHKB)
ENST00000468532.5:n.325-87C>G (CHKB)
ENST00000476289.5:n.721-87C>G (CHKB)
ENST00000479003.5:n.1073-87C>G (CHKB)
ENST00000481673.5:n.898-87C>G (CHKB)
ENST00000484266.5:n.576+609C>G (CHKB)
ENST00000492556.5:n.1218-87C>G (CHKB-CPT1B)
ENST00000492582.5:n.1107-87C>G (CHKB)