Canonical Allele Identifier: CA2008891741
Gene: ST14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.130209652C= , CM000673.2:g.130209652C= GRCh38
NC_000011.9:g.130079547C= , CM000673.1:g.130079547C= GRCh37
NC_000011.8:g.129584757C= NCBI36
NG_012132.1:g.54866C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278742.6:c.2407-10C= MANE Select ENSP00000278742.5:n.2407-10C=
ENST00000278742.5:c.2407-10C= ENSP00000278742.5:n.2407-10C=
NM_021978.3:c.2407-10C= NP_068813.1:n.2407-10C=
NM_021978.4:c.2407-10C= MANE Select NP_068813.1:n.2407-10C=