Canonical Allele Identifier: CA391768822
Gene: CHST14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472265T>G , CM000677.2:g.40472265T>G GRCh38
NC_000015.9:g.40764464T>G , CM000677.1:g.40764464T>G GRCh37
NC_000015.8:g.38551756T>G NCBI36
NG_017074.1:g.6305T>G , LRG_600:g.6305T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.1052T>G MANE Select ENSP00000307297.6:p.Val351Gly
ENST00000306243.6:c.1052T>G ENSP00000307297.5:p.Val351Gly
ENST00000559991.1:c.977T>G ENSP00000453882.1:p.Val326Gly
NM_130468.3:c.1052T>G , LRG_600t1:c.1052T>G NP_569735.1:p.Val351Gly
NM_130468.4:c.1052T>G MANE Select NP_569735.1:p.Val351Gly