Canonical Allele Identifier: CA151133
Gene: ST14 HGNC NCBI

Linked Data

ClinVar Variation Id: 126420
ClinVar RCV Id: RCV000114360
dbSNP Id: rs587777263

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.130208449del , CM000673.2:g.130208449del GRCh38
NC_000011.9:g.130078344del , CM000673.1:g.130078344del GRCh37
NC_000011.8:g.129583554del NCBI36
NG_012132.1:g.53663del

Transcript Alleles

HGVS Amino-acid change
ENST00000278742.6:c.2034del MANE Select ENSP00000278742.5:p.Leu678PhefsTer?
ENST00000278742.5:c.2034del ENSP00000278742.5:p.Leu678PhefsTer?
NM_021978.3:c.2034del NP_068813.1:p.Leu678PhefsTer?
NM_021978.4:c.2034del MANE Select NP_068813.1:p.Leu678PhefsTer?