Canonical Allele Identifier: CA391769065
Gene: CHST14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472319T>A , CM000677.2:g.40472319T>A GRCh38
NC_000015.9:g.40764518T>A , CM000677.1:g.40764518T>A GRCh37
NC_000015.8:g.38551810T>A NCBI36
NG_017074.1:g.6359T>A , LRG_600:g.6359T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.1106T>A MANE Select ENSP00000307297.6:p.Val369Asp
ENST00000306243.6:c.1106T>A ENSP00000307297.5:p.Val369Asp
ENST00000559991.1:c.1031T>A ENSP00000453882.1:p.Val344Asp
NM_130468.3:c.1106T>A , LRG_600t1:c.1106T>A NP_569735.1:p.Val369Asp
NM_130468.4:c.1106T>A MANE Select NP_569735.1:p.Val369Asp