Canonical Allele Identifier: CA391768976
Gene: CHST14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472299T>A , CM000677.2:g.40472299T>A GRCh38
NC_000015.9:g.40764498T>A , CM000677.1:g.40764498T>A GRCh37
NC_000015.8:g.38551790T>A NCBI36
NG_017074.1:g.6339T>A , LRG_600:g.6339T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.1086T>A MANE Select ENSP00000307297.6:p.Phe362Leu
ENST00000306243.6:c.1086T>A ENSP00000307297.5:p.Phe362Leu
ENST00000559991.1:c.1011T>A ENSP00000453882.1:p.Phe337Leu
NM_130468.3:c.1086T>A , LRG_600t1:c.1086T>A NP_569735.1:p.Phe362Leu
NM_130468.4:c.1086T>A MANE Select NP_569735.1:p.Phe362Leu