Canonical Allele Identifier: CA482918365

Linked Data

dbSNP Id: rs2137534396
MyVariant Identifiers: chr13:g.23898679G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23324540G>A , CM000675.2:g.23324540G>A GRCh38
NC_000013.10:g.23898679G>A , CM000675.1:g.23898679G>A GRCh37
NC_000013.9:g.22796679G>A NCBI36
NG_008759.1:g.148620G>A , LRG_207:g.148620G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2186-12425C>T (SACS) ENSP00000508399.1:n.2186-12425C>T
ENST00000683210.1:c.2185+29245C>T (SACS) ENSP00000506739.1:n.2185+29245C>T
ENST00000684325.1:c.2186-2866C>T (SACS) ENSP00000508121.1:n.2186-2866C>T
ENST00000684497.1:c.2186-1896C>T (SACS) ENSP00000507057.1:n.2186-1896C>T
ENST00000218867.4:c.875G>A (SGCG) MANE Select ENSP00000218867.3:p.Ter292=
ENST00000218867.3:c.875G>A (SGCG) ENSP00000218867.3:p.Ter292=
NM_000231.2:c.875G>A , LRG_207t1:c.875G>A (SGCG) NP_000222.1:p.Ter292=
XM_005266505.2:c.875G>A (SGCG) XP_005266562.1:p.Ter292=
XM_006719861.2:c.929G>A (SGCG) XP_006719924.1:p.Ter310=
XM_006719861.3:c.929G>A (SGCG) XP_006719924.1:p.Ter310=
XM_024449397.1:c.875G>A (SGCG) XP_024305165.1:p.Ter292=
NM_000231.3:c.875G>A (SGCG) MANE Select NP_000222.2:p.Ter292=
NM_001378244.1:c.929G>A (SGCG) NP_001365173.1:p.Ter310=
NM_001378245.1:c.875G>A (SGCG) NP_001365174.1:p.Ter292=
NM_001378246.1:c.875G>A (SGCG) NP_001365175.1:p.Ter292=