Canonical Allele Identifier: CA2627824998
Gene: CHST14 HGNC NCBI

Linked Data

gnomAD v4: 15-40472347-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472347A>T , CM000677.2:g.40472347A>T GRCh38
NC_000015.9:g.40764546A>T , CM000677.1:g.40764546A>T GRCh37
NC_000015.8:g.38551838A>T NCBI36
NG_017074.1:g.6387A>T , LRG_600:g.6387A>T

Transcript Alleles

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