Canonical Allele Identifier: CA2171795563

Gene: CHST14

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40472517_40472518delinsAG , CM000677.2:g.40472517_40472518delinsAG	GRCh38
NC_000015.9:g.40764716_40764717delinsAG , CM000677.1:g.40764716_40764717delinsAG	GRCh37
NC_000015.8:g.38552008_38552009delinsAG	NCBI36
NG_017074.1:g.6557_6558delinsAG , LRG_600:g.6557_6558delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.*173_*174delinsAG MANE Select	ENSP00000307297.6:n.*173_*174delinsAG
ENST00000306243.6:c.*173_*174delinsAG	ENSP00000307297.5:n.*173_*174delinsAG
ENST00000559991.1:c.*173_*174delinsAG	ENSP00000453882.1:n.*173_*174delinsAG
NM_130468.3:c.*173_*174delinsAG , LRG_600t1:c.*173_*174delinsAG	NP_569735.1:n.*173_*174delinsAG
NM_130468.4:c.*173_*174delinsAG MANE Select	NP_569735.1:n.*173_*174delinsAG