Canonical Allele Identifier: CA391768877
Gene: CHST14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.40764476A>C (hg19) chr15:g.40472277A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472277A>C , CM000677.2:g.40472277A>C GRCh38
NC_000015.9:g.40764476A>C , CM000677.1:g.40764476A>C GRCh37
NC_000015.8:g.38551768A>C NCBI36
NG_017074.1:g.6317A>C , LRG_600:g.6317A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.1064A>C MANE Select ENSP00000307297.6:p.Tyr355Ser
ENST00000306243.6:c.1064A>C ENSP00000307297.5:p.Tyr355Ser
ENST00000559991.1:c.989A>C ENSP00000453882.1:p.Tyr330Ser
NM_130468.3:c.1064A>C , LRG_600t1:c.1064A>C NP_569735.1:p.Tyr355Ser
NM_130468.4:c.1064A>C MANE Select NP_569735.1:p.Tyr355Ser
Search 100 bp 5'
Search 100 bp 3'