Canonical Allele Identifier: CA2171795585
Gene: CHST14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472555T= , CM000677.2:g.40472555T= GRCh38
NC_000015.9:g.40764754T= , CM000677.1:g.40764754T= GRCh37
NC_000015.8:g.38552046T= NCBI36
NG_017074.1:g.6595T= , LRG_600:g.6595T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.*211T= MANE Select ENSP00000307297.6:n.*211T=
ENST00000306243.6:c.*211T= ENSP00000307297.5:n.*211T=
ENST00000559991.1:c.*211T= ENSP00000453882.1:n.*211T=
NM_130468.3:c.*211T= , LRG_600t1:c.*211T= NP_569735.1:n.*211T=
NM_130468.4:c.*211T= MANE Select NP_569735.1:n.*211T=
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