Canonical Allele Identifier: CA2008891700
Gene: ST14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.130209640G= , CM000673.2:g.130209640G= GRCh38
NC_000011.9:g.130079535G= , CM000673.1:g.130079535G= GRCh37
NC_000011.8:g.129584745G= NCBI36
NG_012132.1:g.54854G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278742.6:c.2407-22G= MANE Select ENSP00000278742.5:n.2407-22G=
ENST00000278742.5:c.2407-22G= ENSP00000278742.5:n.2407-22G=
NM_021978.3:c.2407-22G= NP_068813.1:n.2407-22G=
NM_021978.4:c.2407-22G= MANE Select NP_068813.1:n.2407-22G=