Canonical Allele Identifier: CA2171795516
Gene: CHST14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472413A= , CM000677.2:g.40472413A= GRCh38
NC_000015.9:g.40764612A= , CM000677.1:g.40764612A= GRCh37
NC_000015.8:g.38551904A= NCBI36
NG_017074.1:g.6453A= , LRG_600:g.6453A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.*69A= MANE Select ENSP00000307297.6:n.*69A=
ENST00000306243.6:c.*69A= ENSP00000307297.5:n.*69A=
ENST00000559991.1:c.*69A= ENSP00000453882.1:n.*69A=
NM_130468.3:c.*69A= , LRG_600t1:c.*69A= NP_569735.1:n.*69A=
NM_130468.4:c.*69A= MANE Select NP_569735.1:n.*69A=