Canonical Allele Identifier: CA2171795564

Gene: CHST14

Linked Data

• dbSNP Id: rs1894365683

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40472518del , CM000677.2:g.40472518del	GRCh38
NC_000015.9:g.40764717del , CM000677.1:g.40764717del	GRCh37
NC_000015.8:g.38552009del	NCBI36
NG_017074.1:g.6558del , LRG_600:g.6558del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.*174del MANE Select	ENSP00000307297.6:n.*174del
ENST00000306243.6:c.*174del	ENSP00000307297.5:n.*174del
ENST00000559991.1:c.*174del	ENSP00000453882.1:n.*174del
NM_130468.3:c.*174del , LRG_600t1:c.*174del	NP_569735.1:n.*174del
NM_130468.4:c.*174del MANE Select	NP_569735.1:n.*174del