Canonical Allele Identifier: CA391762126
Gene: CHST14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40471296G>C , CM000677.2:g.40471296G>C GRCh38
NC_000015.9:g.40763495G>C , CM000677.1:g.40763495G>C GRCh37
NC_000015.8:g.38550787G>C NCBI36
NG_017074.1:g.5336G>C , LRG_600:g.5336G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.83G>C MANE Select ENSP00000307297.6:p.Gly28Ala
ENST00000306243.6:c.83G>C ENSP00000307297.5:p.Gly28Ala
ENST00000559991.1:c.83G>C ENSP00000453882.1:p.Gly28Ala
NM_130468.3:c.83G>C , LRG_600t1:c.83G>C NP_569735.1:p.Gly28Ala
NM_130468.4:c.83G>C MANE Select NP_569735.1:p.Gly28Ala