Canonical Allele Identifier: CA2772523014
Gene: SOBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.107634499_107634500dup , CM000668.2:g.107634499_107634500dup GRCh38
NC_000006.11:g.107955703_107955704dup , CM000668.1:g.107955703_107955704dup GRCh37
NC_000006.10:g.108062396_108062397dup NCBI36
NG_028200.1:g.149387_149388dup
NG_028200.2:g.149387_149388dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000317357.10:c.1655_1656dup MANE Select ENSP00000318900.5:p.Asn553ProfsTer?
ENST00000317357.9:c.1655_1656dup ENSP00000318900.5:p.Asn553ProfsTer?
NM_018013.3:c.1655_1656dup NP_060483.3:p.Asn553ProfsTer?
XM_005267041.3:c.1808_1809dup XP_005267098.1:p.Asn604ProfsTer?
XM_005267042.3:c.1712_1713dup XP_005267099.1:p.Asn572ProfsTer?
XM_011535920.1:c.1808_1809dup XP_011534222.1:p.Asn604ProfsTer?
XM_011535921.1:c.1694_1695dup XP_011534223.1:p.Asn566ProfsTer?
XM_011535922.1:c.1067_1068dup XP_011534224.1:p.Asn357ProfsTer?
XM_011535923.1:c.878_879dup XP_011534225.1:p.Asn294ProfsTer?
XM_005267041.4:c.1808_1809dup XP_005267098.1:p.Asn604ProfsTer?
XM_005267042.4:c.1712_1713dup XP_005267099.1:p.Asn572ProfsTer?
XM_011535920.2:c.1808_1809dup XP_011534222.1:p.Asn604ProfsTer?
XM_011535921.2:c.1694_1695dup XP_011534223.1:p.Asn566ProfsTer?
XM_011535923.2:c.878_879dup XP_011534225.1:p.Asn294ProfsTer?
XM_017010991.1:c.1208_1209dup XP_016866480.1:p.Asn404ProfsTer?
XM_017010992.1:c.1208_1209dup XP_016866481.1:p.Asn404ProfsTer?
XM_017010993.1:c.1208_1209dup XP_016866482.1:p.Asn404ProfsTer?
XM_017010994.1:c.1208_1209dup XP_016866483.1:p.Asn404ProfsTer?
NM_018013.4:c.1655_1656dup MANE Select NP_060483.3:p.Asn553ProfsTer?