Canonical Allele Identifier: CA391769071
Gene: CHST14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472321A>C , CM000677.2:g.40472321A>C GRCh38
NC_000015.9:g.40764520A>C , CM000677.1:g.40764520A>C GRCh37
NC_000015.8:g.38551812A>C NCBI36
NG_017074.1:g.6361A>C , LRG_600:g.6361A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.1108A>C MANE Select ENSP00000307297.6:p.Thr370Pro
ENST00000306243.6:c.1108A>C ENSP00000307297.5:p.Thr370Pro
ENST00000559991.1:c.1033A>C ENSP00000453882.1:p.Thr345Pro
NM_130468.3:c.1108A>C , LRG_600t1:c.1108A>C NP_569735.1:p.Thr370Pro
NM_130468.4:c.1108A>C MANE Select NP_569735.1:p.Thr370Pro