Canonical Allele Identifier: CA1654172069
Gene: OSTM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108074627G= , CM000668.2:g.108074627G= GRCh38
NC_000006.11:g.108395831G= , CM000668.1:g.108395831G= GRCh37
NC_000006.10:g.108502524G= NCBI36
NG_007262.1:g.5111C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000467960.2:c.25C= ENSP00000514449.1:p.Gln9=
ENST00000492130.2:c.25C= ENSP00000514453.1:p.Gln9=
ENST00000699569.1:c.25C= ENSP00000514443.1:p.Gln9=
ENST00000699572.1:c.25C= ENSP00000514444.1:p.Gln9=
ENST00000699573.1:c.25C= ENSP00000514445.1:p.Gln9=
ENST00000699574.1:c.25C= ENSP00000514446.1:p.Gln9=
ENST00000699575.1:c.25C= ENSP00000514447.1:p.Gln9=
ENST00000699576.1:c.25C= ENSP00000514448.1:p.Gln9=
ENST00000699577.1:c.25C= ENSP00000514450.1:p.Gln9=
ENST00000699578.1:c.25C= ENSP00000514451.1:p.Gln9=
ENST00000699579.1:c.25C= ENSP00000514452.1:p.Gln9=
ENST00000699580.1:c.-40+432C= ENSP00000514454.1:n.-40+432C=
ENST00000699581.1:c.-39-10328C= ENSP00000514455.1:n.-39-10328C=
ENST00000699582.1:n.125C=
ENST00000193322.8:c.25C= MANE Select ENSP00000193322.3:p.Gln9=
ENST00000193322.7:c.25C= ENSP00000193322.3:p.Gln9=
ENST00000440575.6:c.-39-10328C= ENSP00000398556.2:n.-39-10328C=
ENST00000467960.1:n.115C=
NM_014028.3:c.25C= NP_054747.2:p.Gln9=
XM_011535775.1:c.25C= XP_011534077.1:p.Gln9=
XR_942410.1:n.108C=
XR_942410.3:n.107C=
NM_014028.4:c.25C= MANE Select NP_054747.2:p.Gln9=