Canonical Allele Identifier: CA2171795496
Gene: CHST14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472357G= , CM000677.2:g.40472357G= GRCh38
NC_000015.9:g.40764556G= , CM000677.1:g.40764556G= GRCh37
NC_000015.8:g.38551848G= NCBI36
NG_017074.1:g.6397G= , LRG_600:g.6397G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.*13G= MANE Select ENSP00000307297.6:n.*13G=
ENST00000306243.6:c.*13G= ENSP00000307297.5:n.*13G=
ENST00000559991.1:c.*13G= ENSP00000453882.1:n.*13G=
NM_130468.3:c.*13G= , LRG_600t1:c.*13G= NP_569735.1:n.*13G=
NM_130468.4:c.*13G= MANE Select NP_569735.1:n.*13G=