Canonical Allele Identifier: CA1139926514
Gene: SDC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.30874473G= , CM000663.2:g.30874473G= GRCh38
NC_000001.10:g.31347320G= , CM000663.1:g.31347320G= GRCh37
NC_000001.9:g.31119907G= NCBI36
NG_013371.1:g.39161C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000339394.7:c.986C= MANE Select ENSP00000344468.6:p.Thr329=
ENST00000336798.11:c.812C= ENSP00000338346.7:p.Thr271=
ENST00000339394.6:c.986C= ENSP00000344468.6:p.Thr329=
NM_014654.3:c.986C= NP_055469.3:p.Thr329=
XM_011542462.1:c.989C= XP_011540764.1:p.Thr330=
XM_011542463.1:c.953C= XP_011540765.1:p.Thr318=
XM_011542464.1:c.950C= XP_011540766.1:p.Thr317=
XM_011542465.1:c.911C= XP_011540767.1:p.Thr304=
XM_011542466.1:c.860C= XP_011540768.1:p.Thr287=
XM_011542464.2:c.950C= XP_011540766.1:p.Thr317=
NM_014654.4:c.986C= MANE Select NP_055469.3:p.Thr329=