Canonical Allele Identifier: CA2171795521
Gene: CHST14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472431T= , CM000677.2:g.40472431T= GRCh38
NC_000015.9:g.40764630T= , CM000677.1:g.40764630T= GRCh37
NC_000015.8:g.38551922T= NCBI36
NG_017074.1:g.6471T= , LRG_600:g.6471T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.*87T= MANE Select ENSP00000307297.6:n.*87T=
ENST00000306243.6:c.*87T= ENSP00000307297.5:n.*87T=
ENST00000559991.1:c.*87T= ENSP00000453882.1:n.*87T=
NM_130468.3:c.*87T= , LRG_600t1:c.*87T= NP_569735.1:n.*87T=
NM_130468.4:c.*87T= MANE Select NP_569735.1:n.*87T=