Canonical Allele Identifier: CA2171795494
Gene: CHST14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472352T= , CM000677.2:g.40472352T= GRCh38
NC_000015.9:g.40764551T= , CM000677.1:g.40764551T= GRCh37
NC_000015.8:g.38551843T= NCBI36
NG_017074.1:g.6392T= , LRG_600:g.6392T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.*8T= MANE Select ENSP00000307297.6:n.*8T=
ENST00000306243.6:c.*8T= ENSP00000307297.5:n.*8T=
ENST00000559991.1:c.*8T= ENSP00000453882.1:n.*8T=
NM_130468.3:c.*8T= , LRG_600t1:c.*8T= NP_569735.1:n.*8T=
NM_130468.4:c.*8T= MANE Select NP_569735.1:n.*8T=