Canonical Allele Identifier: CA2575679827
Gene: CHST14 HGNC NCBI

Linked Data

gnomAD v4: 15-40472385-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472385A>T , CM000677.2:g.40472385A>T GRCh38
NC_000015.9:g.40764584A>T , CM000677.1:g.40764584A>T GRCh37
NC_000015.8:g.38551876A>T NCBI36
NG_017074.1:g.6425A>T , LRG_600:g.6425A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.*41A>T MANE Select ENSP00000307297.6:n.*41A>T
ENST00000306243.6:c.*41A>T ENSP00000307297.5:n.*41A>T
ENST00000559991.1:c.*41A>T ENSP00000453882.1:n.*41A>T
NM_130468.3:c.*41A>T , LRG_600t1:c.*41A>T NP_569735.1:n.*41A>T
NM_130468.4:c.*41A>T MANE Select NP_569735.1:n.*41A>T
Search 100 bp 5'
Search 100 bp 3'