Canonical Allele Identifier: CA412202666

Gene: CHKB CHKB-CPT1B

Linked Data

• MyVariant Identifiers: chr22:g.51020773T>A (hg19) ; chr22:g.50582344T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50582344T>A , CM000684.2:g.50582344T>A	GRCh38
NC_000022.10:g.51020773T>A , CM000684.1:g.51020773T>A	GRCh37
NC_000022.9:g.49367639T>A	NCBI36
NG_012643.1:g.1324A>T
NG_029213.1:g.5656A>T , LRG_855:g.5656A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406938.3:c.238A>T (CHKB) MANE Select	ENSP00000384400.3:p.Asn80Tyr
ENST00000406938.2:c.238A>T (CHKB)	ENSP00000384400.2:p.Asn80Tyr
ENST00000463053.1:n.320A>T (CHKB)
ENST00000465842.1:n.77A>T (CHKB)
ENST00000468532.5:n.115A>T (CHKB)
ENST00000476289.5:n.511A>T (CHKB)
ENST00000479003.5:n.477A>T (CHKB)
ENST00000481673.5:n.302A>T (CHKB)
ENST00000484266.5:n.481A>T (CHKB)
ENST00000492556.5:n.622A>T (CHKB-CPT1B)
ENST00000492582.5:n.511A>T (CHKB)
NM_005198.4:c.238A>T , LRG_855t1:c.238A>T (CHKB)	NP_005189.2:p.Asn80Tyr
NR_027928.2:n.456A>T (CHKB-CPT1B)
NM_005198.5:c.238A>T (CHKB) MANE Select	NP_005189.2:p.Asn80Tyr