Canonical Allele Identifier: CA391767029
Gene: CHST14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.40764191T>C (hg19) chr15:g.40471992T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40471992T>C , CM000677.2:g.40471992T>C GRCh38
NC_000015.9:g.40764191T>C , CM000677.1:g.40764191T>C GRCh37
NC_000015.8:g.38551483T>C NCBI36
NG_017074.1:g.6032T>C , LRG_600:g.6032T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000306243.7:c.779T>C MANE Select ENSP00000307297.6:p.Phe260Ser
ENST00000306243.6:c.779T>C ENSP00000307297.5:p.Phe260Ser
ENST00000559991.1:c.704T>C ENSP00000453882.1:p.Phe235Ser
NM_130468.3:c.779T>C , LRG_600t1:c.779T>C NP_569735.1:p.Phe260Ser
NM_130468.4:c.779T>C MANE Select NP_569735.1:p.Phe260Ser
Search 100 bp 5'
Search 100 bp 3'