Canonical Allele Identifier: CA391762091
Gene: CHST14 HGNC NCBI

Linked Data

gnomAD v4: 15-40471287-C-T
MyVariant Identifiers: chr15:g.40763486C>T (hg19) chr15:g.40471287C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40471287C>T , CM000677.2:g.40471287C>T GRCh38
NC_000015.9:g.40763486C>T , CM000677.1:g.40763486C>T GRCh37
NC_000015.8:g.38550778C>T NCBI36
NG_017074.1:g.5327C>T , LRG_600:g.5327C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000306243.7:c.74C>T MANE Select ENSP00000307297.6:p.Ala25Val
ENST00000306243.6:c.74C>T ENSP00000307297.5:p.Ala25Val
ENST00000559991.1:c.74C>T ENSP00000453882.1:p.Ala25Val
NM_130468.3:c.74C>T , LRG_600t1:c.74C>T NP_569735.1:p.Ala25Val
NM_130468.4:c.74C>T MANE Select NP_569735.1:p.Ala25Val
Search 100 bp 5'
Search 100 bp 3'