Canonical Allele Identifier: CA391767077
Gene: CHST14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.40764200T>C (hg19) chr15:g.40472001T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472001T>C , CM000677.2:g.40472001T>C GRCh38
NC_000015.9:g.40764200T>C , CM000677.1:g.40764200T>C GRCh37
NC_000015.8:g.38551492T>C NCBI36
NG_017074.1:g.6041T>C , LRG_600:g.6041T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000306243.7:c.788T>C MANE Select ENSP00000307297.6:p.Phe263Ser
ENST00000306243.6:c.788T>C ENSP00000307297.5:p.Phe263Ser
ENST00000559991.1:c.713T>C ENSP00000453882.1:p.Phe238Ser
NM_130468.3:c.788T>C , LRG_600t1:c.788T>C NP_569735.1:p.Phe263Ser
NM_130468.4:c.788T>C MANE Select NP_569735.1:p.Phe263Ser
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