Canonical Allele Identifier: CA15745806
Gene: SOX5 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs146039840

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.23949682T>G , CM000674.2:g.23949682T>G GRCh38
NC_000012.10:g.23993883T>G NCBI36
NC_000012.11:g.24102616T>G , CM000674.1:g.24102616T>G GRCh37
NG_029612.1:g.617765A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367206.7:c.8+1187A>C ENSP00000356174.3:p.=
ENST00000381381.6:c.-120A>C ENSP00000370788.2:p.=
ENST00000441133.2:c.-60-21A>C ENSP00000393240.2:p.=
ENST00000451604.6:c.-81A>C ENSP00000398273.2:p.=
ENST00000541847.5:c.8+1187A>C ENSP00000442119.1:p.=
ENST00000545921.5:c.8+1187A>C ENSP00000443520.1:p.=
NM_001261414.1:c.-1-53658A>C VV NP_001248343.1:p.=
NM_001261415.1:c.8+1187A>C VV NP_001248344.1:p.=
NM_006940.4:c.-81A>C VV NP_008871.3:p.=
NM_152989.3:c.-1-53658A>C VV NP_694534.1:p.=
XM_006719149.2:c.-1-53658A>C XP_006719212.1:p.=
XM_011520833.1:c.8+1187A>C XP_011519135.1:p.=
XM_011520834.1:c.-1-53658A>C XP_011519136.1:p.=
XM_011520835.1:c.-1-53658A>C XP_011519137.1:p.=
XM_011520836.1:c.1-53659A>C XP_011519138.1:p.=
XM_011520839.1:c.-1-53658A>C XP_011519141.1:p.=