Canonical Allele Identifier: CA391768839
Gene: CHST14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40472270C>T , CM000677.2:g.40472270C>T GRCh38
NC_000015.9:g.40764469C>T , CM000677.1:g.40764469C>T GRCh37
NC_000015.8:g.38551761C>T NCBI36
NG_017074.1:g.6310C>T , LRG_600:g.6310C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000306243.7:c.1057C>T MANE Select ENSP00000307297.6:p.Pro353Ser
ENST00000306243.6:c.1057C>T ENSP00000307297.5:p.Pro353Ser
ENST00000559991.1:c.982C>T ENSP00000453882.1:p.Pro328Ser
NM_130468.3:c.1057C>T , LRG_600t1:c.1057C>T NP_569735.1:p.Pro353Ser
NM_130468.4:c.1057C>T MANE Select NP_569735.1:p.Pro353Ser