Canonical Allele Identifier: CA391762092
Gene: CHST14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.40763488C>A (hg19) chr15:g.40471289C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40471289C>A , CM000677.2:g.40471289C>A GRCh38
NC_000015.9:g.40763488C>A , CM000677.1:g.40763488C>A GRCh37
NC_000015.8:g.38550780C>A NCBI36
NG_017074.1:g.5329C>A , LRG_600:g.5329C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.76C>A MANE Select ENSP00000307297.6:p.Pro26Thr
ENST00000306243.6:c.76C>A ENSP00000307297.5:p.Pro26Thr
ENST00000559991.1:c.76C>A ENSP00000453882.1:p.Pro26Thr
NM_130468.3:c.76C>A , LRG_600t1:c.76C>A NP_569735.1:p.Pro26Thr
NM_130468.4:c.76C>A MANE Select NP_569735.1:p.Pro26Thr
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