Canonical Allele Identifier: CA2171795355
Gene: CHST14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472002C= , CM000677.2:g.40472002C= GRCh38
NC_000015.9:g.40764201C= , CM000677.1:g.40764201C= GRCh37
NC_000015.8:g.38551493C= NCBI36
NG_017074.1:g.6042C= , LRG_600:g.6042C=

Transcript Alleles

HGVS Amino-acid change
ENST00000306243.7:c.789C= MANE Select ENSP00000307297.6:p.Phe263=
ENST00000306243.6:c.789C= ENSP00000307297.5:p.Phe263=
ENST00000559991.1:c.714C= ENSP00000453882.1:p.Phe238=
NM_130468.3:c.789C= , LRG_600t1:c.789C= NP_569735.1:p.Phe263=
NM_130468.4:c.789C= MANE Select NP_569735.1:p.Phe263=