Canonical Allele Identifier: CA2171795543
Gene: CHST14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472471C= , CM000677.2:g.40472471C= GRCh38
NC_000015.9:g.40764670C= , CM000677.1:g.40764670C= GRCh37
NC_000015.8:g.38551962C= NCBI36
NG_017074.1:g.6511C= , LRG_600:g.6511C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.*127C= MANE Select ENSP00000307297.6:n.*127C=
ENST00000306243.6:c.*127C= ENSP00000307297.5:n.*127C=
ENST00000559991.1:c.*127C= ENSP00000453882.1:n.*127C=
NM_130468.3:c.*127C= , LRG_600t1:c.*127C= NP_569735.1:n.*127C=
NM_130468.4:c.*127C= MANE Select NP_569735.1:n.*127C=