Canonical Allele Identifier: CA365171257
Gene: SOBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.107634615T>G , CM000668.2:g.107634615T>G GRCh38
NC_000006.11:g.107955819T>G , CM000668.1:g.107955819T>G GRCh37
NC_000006.10:g.108062512T>G NCBI36
NG_028200.1:g.149503T>G
NG_028200.2:g.149503T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000317357.10:c.1771T>G MANE Select ENSP00000318900.5:p.Ser591Ala
ENST00000317357.9:c.1771T>G ENSP00000318900.5:p.Ser591Ala
NM_018013.3:c.1771T>G NP_060483.3:p.Ser591Ala
XM_005267041.3:c.1924T>G XP_005267098.1:p.Ser642Ala
XM_005267042.3:c.1828T>G XP_005267099.1:p.Ser610Ala
XM_011535920.1:c.1924T>G XP_011534222.1:p.Ser642Ala
XM_011535921.1:c.1810T>G XP_011534223.1:p.Ser604Ala
XM_011535922.1:c.1183T>G XP_011534224.1:p.Ser395Ala
XM_011535923.1:c.994T>G XP_011534225.1:p.Ser332Ala
XM_005267041.4:c.1924T>G XP_005267098.1:p.Ser642Ala
XM_005267042.4:c.1828T>G XP_005267099.1:p.Ser610Ala
XM_011535920.2:c.1924T>G XP_011534222.1:p.Ser642Ala
XM_011535921.2:c.1810T>G XP_011534223.1:p.Ser604Ala
XM_011535923.2:c.994T>G XP_011534225.1:p.Ser332Ala
XM_017010991.1:c.1324T>G XP_016866480.1:p.Ser442Ala
XM_017010992.1:c.1324T>G XP_016866481.1:p.Ser442Ala
XM_017010993.1:c.1324T>G XP_016866482.1:p.Ser442Ala
XM_017010994.1:c.1324T>G XP_016866483.1:p.Ser442Ala
NM_018013.4:c.1771T>G MANE Select NP_060483.3:p.Ser591Ala