Canonical Allele Identifier: CA2679876742
Gene: SOBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.107634464_107634475dup , CM000668.2:g.107634464_107634475dup GRCh38
NC_000006.11:g.107955668_107955679dup , CM000668.1:g.107955668_107955679dup GRCh37
NC_000006.10:g.108062361_108062372dup NCBI36
NG_028200.1:g.149352_149363dup
NG_028200.2:g.149352_149363dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000317357.10:c.1620_1631dup MANE Select ENSP00000318900.5:p.Pro544_His545insIleProIlePro
ENST00000317357.9:c.1620_1631dup ENSP00000318900.5:p.Pro544_His545insIleProIlePro
NM_018013.3:c.1620_1631dup NP_060483.3:p.Pro544_His545insIleProIlePro
XM_005267041.3:c.1773_1784dup XP_005267098.1:p.Pro595_His596insIleProIlePro
XM_005267042.3:c.1677_1688dup XP_005267099.1:p.Pro563_His564insIleProIlePro
XM_011535920.1:c.1773_1784dup XP_011534222.1:p.Pro595_His596insIleProIlePro
XM_011535921.1:c.1659_1670dup XP_011534223.1:p.Pro557_His558insIleProIlePro
XM_011535922.1:c.1032_1043dup XP_011534224.1:p.Pro348_His349insIleProIlePro
XM_011535923.1:c.843_854dup XP_011534225.1:p.Pro285_His286insIleProIlePro
XM_005267041.4:c.1773_1784dup XP_005267098.1:p.Pro595_His596insIleProIlePro
XM_005267042.4:c.1677_1688dup XP_005267099.1:p.Pro563_His564insIleProIlePro
XM_011535920.2:c.1773_1784dup XP_011534222.1:p.Pro595_His596insIleProIlePro
XM_011535921.2:c.1659_1670dup XP_011534223.1:p.Pro557_His558insIleProIlePro
XM_011535923.2:c.843_854dup XP_011534225.1:p.Pro285_His286insIleProIlePro
XM_017010991.1:c.1173_1184dup XP_016866480.1:p.Pro395_His396insIleProIlePro
XM_017010992.1:c.1173_1184dup XP_016866481.1:p.Pro395_His396insIleProIlePro
XM_017010993.1:c.1173_1184dup XP_016866482.1:p.Pro395_His396insIleProIlePro
XM_017010994.1:c.1173_1184dup XP_016866483.1:p.Pro395_His396insIleProIlePro
NM_018013.4:c.1620_1631dup MANE Select NP_060483.3:p.Pro544_His545insIleProIlePro