Canonical Allele Identifier: CA2171795487
Gene: CHST14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472332G= , CM000677.2:g.40472332G= GRCh38
NC_000015.9:g.40764531G= , CM000677.1:g.40764531G= GRCh37
NC_000015.8:g.38551823G= NCBI36
NG_017074.1:g.6372G= , LRG_600:g.6372G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.1119G= MANE Select ENSP00000307297.6:p.Ala373=
ENST00000306243.6:c.1119G= ENSP00000307297.5:p.Ala373=
ENST00000559991.1:c.1044G= ENSP00000453882.1:p.Ala348=
NM_130468.3:c.1119G= , LRG_600t1:c.1119G= NP_569735.1:p.Ala373=
NM_130468.4:c.1119G= MANE Select NP_569735.1:p.Ala373=