Canonical Allele Identifier: CA2171795520

Gene: CHST14

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40472423_40472425delinsACT , CM000677.2:g.40472423_40472425delinsACT	GRCh38
NC_000015.9:g.40764622_40764624delinsACT , CM000677.1:g.40764622_40764624delinsACT	GRCh37
NC_000015.8:g.38551914_38551916delinsACT	NCBI36
NG_017074.1:g.6463_6465delinsACT , LRG_600:g.6463_6465delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.*79_*81delinsACT MANE Select	ENSP00000307297.6:n.*79_*81delinsACT
ENST00000306243.6:c.*79_*81delinsACT	ENSP00000307297.5:n.*79_*81delinsACT
ENST00000559991.1:c.*79_*81delinsACT	ENSP00000453882.1:n.*79_*81delinsACT
NM_130468.3:c.*79_*81delinsACT , LRG_600t1:c.*79_*81delinsACT	NP_569735.1:n.*79_*81delinsACT
NM_130468.4:c.*79_*81delinsACT MANE Select	NP_569735.1:n.*79_*81delinsACT