Canonical Allele Identifier: CA1653938893

Gene: SOBP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634591_107634592delinsTC , CM000668.2:g.107634591_107634592delinsTC	GRCh38
NC_000006.11:g.107955795_107955796delinsTC , CM000668.1:g.107955795_107955796delinsTC	GRCh37
NC_000006.10:g.108062488_108062489delinsTC	NCBI36
NG_028200.1:g.149479_149480delinsTC
NG_028200.2:g.149479_149480delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1747_1748delinsTC MANE Select	ENSP00000318900.5:p.Ser583=
ENST00000317357.9:c.1747_1748delinsTC	ENSP00000318900.5:p.Ser583=
NM_018013.3:c.1747_1748delinsTC	NP_060483.3:p.Ser583=
XM_005267041.3:c.1900_1901delinsTC	XP_005267098.1:p.Ser634=
XM_005267042.3:c.1804_1805delinsTC	XP_005267099.1:p.Ser602=
XM_011535920.1:c.1900_1901delinsTC	XP_011534222.1:p.Ser634=
XM_011535921.1:c.1786_1787delinsTC	XP_011534223.1:p.Ser596=
XM_011535922.1:c.1159_1160delinsTC	XP_011534224.1:p.Ser387=
XM_011535923.1:c.970_971delinsTC	XP_011534225.1:p.Ser324=
XM_005267041.4:c.1900_1901delinsTC	XP_005267098.1:p.Ser634=
XM_005267042.4:c.1804_1805delinsTC	XP_005267099.1:p.Ser602=
XM_011535920.2:c.1900_1901delinsTC	XP_011534222.1:p.Ser634=
XM_011535921.2:c.1786_1787delinsTC	XP_011534223.1:p.Ser596=
XM_011535923.2:c.970_971delinsTC	XP_011534225.1:p.Ser324=
XM_017010991.1:c.1300_1301delinsTC	XP_016866480.1:p.Ser434=
XM_017010992.1:c.1300_1301delinsTC	XP_016866481.1:p.Ser434=
XM_017010993.1:c.1300_1301delinsTC	XP_016866482.1:p.Ser434=
XM_017010994.1:c.1300_1301delinsTC	XP_016866483.1:p.Ser434=
NM_018013.4:c.1747_1748delinsTC MANE Select	NP_060483.3:p.Ser583=