Canonical Allele Identifier: CA14093922

Gene: CHSY1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.101241729A>G , CM000677.2:g.101241729A>G	GRCh38
NC_000015.9:g.101781934A>G , CM000677.1:g.101781934A>G	GRCh37
NC_000015.8:g.99599457A>G	NCBI36
NG_031908.1:g.15204T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254190.4:c.321-6152T>C MANE Select	ENSP00000254190.3:n.321-6152T>C
ENST00000254190.3:c.321-6152T>C	ENSP00000254190.3:n.321-6152T>C
ENST00000559384.1:n.70+819T>C
NM_014918.4:c.321-6152T>C	NP_055733.2:n.321-6152T>C
XM_011521364.1:c.321-6152T>C	XP_011519666.1:n.321-6152T>C
XM_011521364.2:c.321-6152T>C	XP_011519666.1:n.321-6152T>C
NM_014918.5:c.321-6152T>C MANE Select	NP_055733.2:n.321-6152T>C