Canonical Allele Identifier: CA391769168
Gene: CHST14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.40764535C>T (hg19) chr15:g.40472336C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472336C>T , CM000677.2:g.40472336C>T GRCh38
NC_000015.9:g.40764535C>T , CM000677.1:g.40764535C>T GRCh37
NC_000015.8:g.38551827C>T NCBI36
NG_017074.1:g.6376C>T , LRG_600:g.6376C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.1123C>T MANE Select ENSP00000307297.6:p.Gln375Ter
ENST00000306243.6:c.1123C>T ENSP00000307297.5:p.Gln375Ter
ENST00000559991.1:c.1048C>T ENSP00000453882.1:p.Gln350Ter
NM_130468.3:c.1123C>T , LRG_600t1:c.1123C>T NP_569735.1:p.Gln375Ter
NM_130468.4:c.1123C>T MANE Select NP_569735.1:p.Gln375Ter
Search 100 bp 5'
Search 100 bp 3'