Canonical Allele Identifier: CA1653939371

Gene: SOBP

Linked Data

• dbSNP Id: rs1770935499

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634853_107634858del , CM000668.2:g.107634853_107634858del	GRCh38
NC_000006.11:g.107956057_107956062del , CM000668.1:g.107956057_107956062del	GRCh37
NC_000006.10:g.108062750_108062755del	NCBI36
NG_028200.1:g.149741_149746del
NG_028200.2:g.149741_149746del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.2009_2014del MANE Select	ENSP00000318900.5:p.Arg670_Ala671del
ENST00000317357.9:c.2009_2014del	ENSP00000318900.5:p.Arg670_Ala671del
NM_018013.3:c.2009_2014del	NP_060483.3:p.Arg670_Ala671del
XM_005267041.3:c.2162_2167del	XP_005267098.1:p.Arg721_Ala722del
XM_005267042.3:c.2066_2071del	XP_005267099.1:p.Arg689_Ala690del
XM_011535920.1:c.2162_2167del	XP_011534222.1:p.Arg721_Ala722del
XM_011535921.1:c.2048_2053del	XP_011534223.1:p.Arg683_Ala684del
XM_011535922.1:c.1421_1426del	XP_011534224.1:p.Arg474_Ala475del
XM_011535923.1:c.1232_1237del	XP_011534225.1:p.Arg411_Ala412del
XM_005267041.4:c.2162_2167del	XP_005267098.1:p.Arg721_Ala722del
XM_005267042.4:c.2066_2071del	XP_005267099.1:p.Arg689_Ala690del
XM_011535920.2:c.2162_2167del	XP_011534222.1:p.Arg721_Ala722del
XM_011535921.2:c.2048_2053del	XP_011534223.1:p.Arg683_Ala684del
XM_011535923.2:c.1232_1237del	XP_011534225.1:p.Arg411_Ala412del
XM_017010991.1:c.1562_1567del	XP_016866480.1:p.Arg521_Ala522del
XM_017010992.1:c.1562_1567del	XP_016866481.1:p.Arg521_Ala522del
XM_017010993.1:c.1562_1567del	XP_016866482.1:p.Arg521_Ala522del
XM_017010994.1:c.1562_1567del	XP_016866483.1:p.Arg521_Ala522del
NM_018013.4:c.2009_2014del MANE Select	NP_060483.3:p.Arg670_Ala671del