Canonical Allele Identifier: CA412202324

Gene: CHKB CHKB-CPT1B

Linked Data

• MyVariant Identifiers: chr22:g.51020703A>T (hg19) ; chr22:g.50582274A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50582274A>T , CM000684.2:g.50582274A>T	GRCh38
NC_000022.10:g.51020703A>T , CM000684.1:g.51020703A>T	GRCh37
NC_000022.9:g.49367569A>T	NCBI36
NG_012643.1:g.1394T>A
NG_029213.1:g.5726T>A , LRG_855:g.5726T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406938.3:c.308T>A (CHKB) MANE Select	ENSP00000384400.3:p.Leu103Gln
ENST00000406938.2:c.308T>A (CHKB)	ENSP00000384400.2:p.Leu103Gln
ENST00000463053.1:n.390T>A (CHKB)
ENST00000465842.1:n.147T>A (CHKB)
ENST00000468532.5:n.185T>A (CHKB)
ENST00000476289.5:n.581T>A (CHKB)
ENST00000479003.5:n.547T>A (CHKB)
ENST00000481673.5:n.372T>A (CHKB)
ENST00000484266.5:n.551T>A (CHKB)
ENST00000492556.5:n.692T>A (CHKB-CPT1B)
ENST00000492582.5:n.581T>A (CHKB)
NM_005198.4:c.308T>A , LRG_855t1:c.308T>A (CHKB)	NP_005189.2:p.Leu103Gln
NR_027928.2:n.526T>A (CHKB-CPT1B)
NM_005198.5:c.308T>A (CHKB) MANE Select	NP_005189.2:p.Leu103Gln