Canonical Allele Identifier: CA1140050753
Gene: SDC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.30874552C= , CM000663.2:g.30874552C= GRCh38
NC_000001.10:g.31347399C= , CM000663.1:g.31347399C= GRCh37
NC_000001.9:g.31119986C= NCBI36
NG_013371.1:g.39082G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000339394.7:c.907G= MANE Select ENSP00000344468.6:p.Asp303=
ENST00000336798.11:c.733G= ENSP00000338346.7:p.Asp245=
ENST00000339394.6:c.907G= ENSP00000344468.6:p.Asp303=
NM_014654.3:c.907G= NP_055469.3:p.Asp303=
XM_011542462.1:c.910G= XP_011540764.1:p.Asp304=
XM_011542463.1:c.874G= XP_011540765.1:p.Asp292=
XM_011542464.1:c.871G= XP_011540766.1:p.Asp291=
XM_011542465.1:c.832G= XP_011540767.1:p.Asp278=
XM_011542466.1:c.781G= XP_011540768.1:p.Asp261=
XM_011542464.2:c.871G= XP_011540766.1:p.Asp291=
NM_014654.4:c.907G= MANE Select NP_055469.3:p.Asp303=