Canonical Allele Identifier: CA2171795522
Gene: CHST14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472432C= , CM000677.2:g.40472432C= GRCh38
NC_000015.9:g.40764631C= , CM000677.1:g.40764631C= GRCh37
NC_000015.8:g.38551923C= NCBI36
NG_017074.1:g.6472C= , LRG_600:g.6472C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.*88C= MANE Select ENSP00000307297.6:n.*88C=
ENST00000306243.6:c.*88C= ENSP00000307297.5:n.*88C=
ENST00000559991.1:c.*88C= ENSP00000453882.1:n.*88C=
NM_130468.3:c.*88C= , LRG_600t1:c.*88C= NP_569735.1:n.*88C=
NM_130468.4:c.*88C= MANE Select NP_569735.1:n.*88C=