Canonical Allele Identifier: CA2679876743
Gene: SOBP HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000317357.10:c.1620del MANE Select ENSP00000318900.5:p.Ile541SerfsTer?
ENST00000317357.9:c.1620del ENSP00000318900.5:p.Ile541SerfsTer?
NM_018013.3:c.1620del NP_060483.3:p.Ile541SerfsTer?
XM_005267041.3:c.1773del XP_005267098.1:p.Ile592SerfsTer?
XM_005267042.3:c.1677del XP_005267099.1:p.Ile560SerfsTer?
XM_011535920.1:c.1773del XP_011534222.1:p.Ile592SerfsTer?
XM_011535921.1:c.1659del XP_011534223.1:p.Ile554SerfsTer?
XM_011535922.1:c.1032del XP_011534224.1:p.Ile345SerfsTer?
XM_011535923.1:c.843del XP_011534225.1:p.Ile282SerfsTer?
XM_005267041.4:c.1773del XP_005267098.1:p.Ile592SerfsTer?
XM_005267042.4:c.1677del XP_005267099.1:p.Ile560SerfsTer?
XM_011535920.2:c.1773del XP_011534222.1:p.Ile592SerfsTer?
XM_011535921.2:c.1659del XP_011534223.1:p.Ile554SerfsTer?
XM_011535923.2:c.843del XP_011534225.1:p.Ile282SerfsTer?
XM_017010991.1:c.1173del XP_016866480.1:p.Ile392SerfsTer?
XM_017010992.1:c.1173del XP_016866481.1:p.Ile392SerfsTer?
XM_017010993.1:c.1173del XP_016866482.1:p.Ile392SerfsTer?
XM_017010994.1:c.1173del XP_016866483.1:p.Ile392SerfsTer?
NM_018013.4:c.1620del MANE Select NP_060483.3:p.Ile541SerfsTer?