Canonical Allele Identifier: CA2008891728
Gene: ST14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.130209650G= , CM000673.2:g.130209650G= GRCh38
NC_000011.9:g.130079545G= , CM000673.1:g.130079545G= GRCh37
NC_000011.8:g.129584755G= NCBI36
NG_012132.1:g.54864G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278742.6:c.2407-12G= MANE Select ENSP00000278742.5:n.2407-12G=
ENST00000278742.5:c.2407-12G= ENSP00000278742.5:n.2407-12G=
NM_021978.3:c.2407-12G= NP_068813.1:n.2407-12G=
NM_021978.4:c.2407-12G= MANE Select NP_068813.1:n.2407-12G=