Canonical Allele Identifier: CA2171795495
Gene: CHST14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472355G= , CM000677.2:g.40472355G= GRCh38
NC_000015.9:g.40764554G= , CM000677.1:g.40764554G= GRCh37
NC_000015.8:g.38551846G= NCBI36
NG_017074.1:g.6395G= , LRG_600:g.6395G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.*11G= MANE Select ENSP00000307297.6:n.*11G=
ENST00000306243.6:c.*11G= ENSP00000307297.5:n.*11G=
ENST00000559991.1:c.*11G= ENSP00000453882.1:n.*11G=
NM_130468.3:c.*11G= , LRG_600t1:c.*11G= NP_569735.1:n.*11G=
NM_130468.4:c.*11G= MANE Select NP_569735.1:n.*11G=