Canonical Allele Identifier: CA489975509
Gene: CHST14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.40764513T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472314T>A , CM000677.2:g.40472314T>A GRCh38
NC_000015.9:g.40764513T>A , CM000677.1:g.40764513T>A GRCh37
NC_000015.8:g.38551805T>A NCBI36
NG_017074.1:g.6354T>A , LRG_600:g.6354T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.1101T>A MANE Select ENSP00000307297.6:p.Pro367=
ENST00000306243.6:c.1101T>A ENSP00000307297.5:p.Pro367=
ENST00000559991.1:c.1026T>A ENSP00000453882.1:p.Pro342=
NM_130468.3:c.1101T>A , LRG_600t1:c.1101T>A NP_569735.1:p.Pro367=
NM_130468.4:c.1101T>A MANE Select NP_569735.1:p.Pro367=
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