Canonical Allele Identifier: CA391769117
Gene: CHST14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.40764527A>G (hg19) chr15:g.40472328A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472328A>G , CM000677.2:g.40472328A>G GRCh38
NC_000015.9:g.40764527A>G , CM000677.1:g.40764527A>G GRCh37
NC_000015.8:g.38551819A>G NCBI36
NG_017074.1:g.6368A>G , LRG_600:g.6368A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.1115A>G MANE Select ENSP00000307297.6:p.Glu372Gly
ENST00000306243.6:c.1115A>G ENSP00000307297.5:p.Glu372Gly
ENST00000559991.1:c.1040A>G ENSP00000453882.1:p.Glu347Gly
NM_130468.3:c.1115A>G , LRG_600t1:c.1115A>G NP_569735.1:p.Glu372Gly
NM_130468.4:c.1115A>G MANE Select NP_569735.1:p.Glu372Gly
Search 100 bp 5'
Search 100 bp 3'