Canonical Allele Identifier: CA1139940232
Gene: SDC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.30876800C= , CM000663.2:g.30876800C= GRCh38
NC_000001.10:g.31349647C= , CM000663.1:g.31349647C= GRCh37
NC_000001.9:g.31122234C= NCBI36
NG_013371.1:g.36834G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000339394.7:c.622G= MANE Select ENSP00000344468.6:p.Val208=
ENST00000336798.11:c.448G= ENSP00000338346.7:p.Val150=
ENST00000339394.6:c.622G= ENSP00000344468.6:p.Val208=
ENST00000471567.1:n.556G=
NM_014654.3:c.622G= NP_055469.3:p.Val208=
XM_011542462.1:c.625G= XP_011540764.1:p.Val209=
XM_011542463.1:c.589G= XP_011540765.1:p.Val197=
XM_011542464.1:c.586G= XP_011540766.1:p.Val196=
XM_011542465.1:c.547G= XP_011540767.1:p.Val183=
XM_011542466.1:c.496G= XP_011540768.1:p.Val166=
XM_011542464.2:c.586G= XP_011540766.1:p.Val196=
NM_014654.4:c.622G= MANE Select NP_055469.3:p.Val208=