Canonical Allele Identifier: CA2171795595
Gene: CHST14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472569G= , CM000677.2:g.40472569G= GRCh38
NC_000015.9:g.40764768G= , CM000677.1:g.40764768G= GRCh37
NC_000015.8:g.38552060G= NCBI36
NG_017074.1:g.6609G= , LRG_600:g.6609G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.*225G= MANE Select ENSP00000307297.6:n.*225G=
ENST00000306243.6:c.*225G= ENSP00000307297.5:n.*225G=
ENST00000559991.1:c.*225G= ENSP00000453882.1:n.*225G=
NM_130468.3:c.*225G= , LRG_600t1:c.*225G= NP_569735.1:n.*225G=
NM_130468.4:c.*225G= MANE Select NP_569735.1:n.*225G=
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