Canonical Allele Identifier: CA391769076
Gene: CHST14 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.40764520A>T (hg19) chr15:g.40472321A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472321A>T , CM000677.2:g.40472321A>T GRCh38
NC_000015.9:g.40764520A>T , CM000677.1:g.40764520A>T GRCh37
NC_000015.8:g.38551812A>T NCBI36
NG_017074.1:g.6361A>T , LRG_600:g.6361A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.1108A>T MANE Select ENSP00000307297.6:p.Thr370Ser
ENST00000306243.6:c.1108A>T ENSP00000307297.5:p.Thr370Ser
ENST00000559991.1:c.1033A>T ENSP00000453882.1:p.Thr345Ser
NM_130468.3:c.1108A>T , LRG_600t1:c.1108A>T NP_569735.1:p.Thr370Ser
NM_130468.4:c.1108A>T MANE Select NP_569735.1:p.Thr370Ser
Search 100 bp 5'
Search 100 bp 3'