Canonical Allele Identifier: CA2171795525

Gene: CHST14

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40472433_40472434delinsTG , CM000677.2:g.40472433_40472434delinsTG	GRCh38
NC_000015.9:g.40764632_40764633delinsTG , CM000677.1:g.40764632_40764633delinsTG	GRCh37
NC_000015.8:g.38551924_38551925delinsTG	NCBI36
NG_017074.1:g.6473_6474delinsTG , LRG_600:g.6473_6474delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.*89_*90delinsTG MANE Select	ENSP00000307297.6:n.*89_*90delinsTG
ENST00000306243.6:c.*89_*90delinsTG	ENSP00000307297.5:n.*89_*90delinsTG
ENST00000559991.1:c.*89_*90delinsTG	ENSP00000453882.1:n.*89_*90delinsTG
NM_130468.3:c.*89_*90delinsTG , LRG_600t1:c.*89_*90delinsTG	NP_569735.1:n.*89_*90delinsTG
NM_130468.4:c.*89_*90delinsTG MANE Select	NP_569735.1:n.*89_*90delinsTG