Canonical Allele Identifier: CA2803858073

Gene: CHST14

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40472568del , CM000677.2:g.40472568del	GRCh38
NC_000015.9:g.40764767del , CM000677.1:g.40764767del	GRCh37
NC_000015.8:g.38552059del	NCBI36
NG_017074.1:g.6608del , LRG_600:g.6608del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306243.7:c.*224del MANE Select	ENSP00000307297.6:n.*224del
ENST00000306243.6:c.*224del	ENSP00000307297.5:n.*224del
ENST00000559991.1:c.*224del	ENSP00000453882.1:n.*224del
NM_130468.3:c.*224del , LRG_600t1:c.*224del	NP_569735.1:n.*224del
NM_130468.4:c.*224del MANE Select	NP_569735.1:n.*224del