Canonical Allele Identifier: CA391768858
Gene: CHST14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.40764473A>T (hg19) chr15:g.40472274A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472274A>T , CM000677.2:g.40472274A>T GRCh38
NC_000015.9:g.40764473A>T , CM000677.1:g.40764473A>T GRCh37
NC_000015.8:g.38551765A>T NCBI36
NG_017074.1:g.6314A>T , LRG_600:g.6314A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.1061A>T MANE Select ENSP00000307297.6:p.Lys354Met
ENST00000306243.6:c.1061A>T ENSP00000307297.5:p.Lys354Met
ENST00000559991.1:c.986A>T ENSP00000453882.1:p.Lys329Met
NM_130468.3:c.1061A>T , LRG_600t1:c.1061A>T NP_569735.1:p.Lys354Met
NM_130468.4:c.1061A>T MANE Select NP_569735.1:p.Lys354Met
Search 100 bp 5'
Search 100 bp 3'