Canonical Allele Identifier: CA2509410972

Gene: SOBP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634726_107634750del , CM000668.2:g.107634726_107634750del	GRCh38
NC_000006.11:g.107955930_107955954del , CM000668.1:g.107955930_107955954del	GRCh37
NC_000006.10:g.108062623_108062647del	NCBI36
NG_028200.1:g.149614_149638del
NG_028200.2:g.149614_149638del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1882_1906del MANE Select	ENSP00000318900.5:p.Gly628ArgfsTer21
ENST00000317357.9:c.1882_1906del	ENSP00000318900.5:p.Gly628ArgfsTer21
NM_018013.3:c.1882_1906del	NP_060483.3:p.Gly628ArgfsTer21
XM_005267041.3:c.2035_2059del	XP_005267098.1:p.Gly679ArgfsTer21
XM_005267042.3:c.1939_1963del	XP_005267099.1:p.Gly647ArgfsTer21
XM_011535920.1:c.2035_2059del	XP_011534222.1:p.Gly679ArgfsTer21
XM_011535921.1:c.1921_1945del	XP_011534223.1:p.Gly641ArgfsTer21
XM_011535922.1:c.1294_1318del	XP_011534224.1:p.Gly432ArgfsTer21
XM_011535923.1:c.1105_1129del	XP_011534225.1:p.Gly369ArgfsTer21
XM_005267041.4:c.2035_2059del	XP_005267098.1:p.Gly679ArgfsTer21
XM_005267042.4:c.1939_1963del	XP_005267099.1:p.Gly647ArgfsTer21
XM_011535920.2:c.2035_2059del	XP_011534222.1:p.Gly679ArgfsTer21
XM_011535921.2:c.1921_1945del	XP_011534223.1:p.Gly641ArgfsTer21
XM_011535923.2:c.1105_1129del	XP_011534225.1:p.Gly369ArgfsTer21
XM_017010991.1:c.1435_1459del	XP_016866480.1:p.Gly479ArgfsTer21
XM_017010992.1:c.1435_1459del	XP_016866481.1:p.Gly479ArgfsTer21
XM_017010993.1:c.1435_1459del	XP_016866482.1:p.Gly479ArgfsTer21
XM_017010994.1:c.1435_1459del	XP_016866483.1:p.Gly479ArgfsTer21
NM_018013.4:c.1882_1906del MANE Select	NP_060483.3:p.Gly628ArgfsTer21