Canonical Allele Identifier: CA391761792
Gene: CHST14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.40763431A>C (hg19) chr15:g.40471232A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40471232A>C , CM000677.2:g.40471232A>C GRCh38
NC_000015.9:g.40763431A>C , CM000677.1:g.40763431A>C GRCh37
NC_000015.8:g.38550723A>C NCBI36
NG_017074.1:g.5272A>C , LRG_600:g.5272A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.19A>C MANE Select ENSP00000307297.6:p.Thr7Pro
ENST00000306243.6:c.19A>C ENSP00000307297.5:p.Thr7Pro
ENST00000559991.1:c.19A>C ENSP00000453882.1:p.Thr7Pro
NM_130468.3:c.19A>C , LRG_600t1:c.19A>C NP_569735.1:p.Thr7Pro
NM_130468.4:c.19A>C MANE Select NP_569735.1:p.Thr7Pro
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