Canonical Allele Identifier: CA2627825005
Gene: CHST14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472358del , CM000677.2:g.40472358del GRCh38
NC_000015.9:g.40764557del , CM000677.1:g.40764557del GRCh37
NC_000015.8:g.38551849del NCBI36
NG_017074.1:g.6398del , LRG_600:g.6398del

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.*14del MANE Select ENSP00000307297.6:n.*14del
ENST00000306243.6:c.*14del ENSP00000307297.5:n.*14del
ENST00000559991.1:c.*14del ENSP00000453882.1:n.*14del
NM_130468.3:c.*14del , LRG_600t1:c.*14del NP_569735.1:n.*14del
NM_130468.4:c.*14del MANE Select NP_569735.1:n.*14del