Canonical Allele Identifier: CA2679876741
Gene: SOBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.107634458del , CM000668.2:g.107634458del GRCh38
NC_000006.11:g.107955662del , CM000668.1:g.107955662del GRCh37
NC_000006.10:g.108062355del NCBI36
NG_028200.1:g.149346del
NG_028200.2:g.149346del

Transcript Alleles

HGVS Amino-acid Change
ENST00000317357.10:c.1614del MANE Select ENSP00000318900.5:p.Ile539SerfsTer?
ENST00000317357.9:c.1614del ENSP00000318900.5:p.Ile539SerfsTer?
NM_018013.3:c.1614del NP_060483.3:p.Ile539SerfsTer?
XM_005267041.3:c.1767del XP_005267098.1:p.Ile590SerfsTer?
XM_005267042.3:c.1671del XP_005267099.1:p.Ile558SerfsTer?
XM_011535920.1:c.1767del XP_011534222.1:p.Ile590SerfsTer?
XM_011535921.1:c.1653del XP_011534223.1:p.Ile552SerfsTer?
XM_011535922.1:c.1026del XP_011534224.1:p.Ile343SerfsTer?
XM_011535923.1:c.837del XP_011534225.1:p.Ile280SerfsTer?
XM_005267041.4:c.1767del XP_005267098.1:p.Ile590SerfsTer?
XM_005267042.4:c.1671del XP_005267099.1:p.Ile558SerfsTer?
XM_011535920.2:c.1767del XP_011534222.1:p.Ile590SerfsTer?
XM_011535921.2:c.1653del XP_011534223.1:p.Ile552SerfsTer?
XM_011535923.2:c.837del XP_011534225.1:p.Ile280SerfsTer?
XM_017010991.1:c.1167del XP_016866480.1:p.Ile390SerfsTer?
XM_017010992.1:c.1167del XP_016866481.1:p.Ile390SerfsTer?
XM_017010993.1:c.1167del XP_016866482.1:p.Ile390SerfsTer?
XM_017010994.1:c.1167del XP_016866483.1:p.Ile390SerfsTer?
NM_018013.4:c.1614del MANE Select NP_060483.3:p.Ile539SerfsTer?