Canonical Allele Identifier: CA1653939158

Gene: SOBP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634718G= , CM000668.2:g.107634718G=	GRCh38
NC_000006.11:g.107955922G= , CM000668.1:g.107955922G=	GRCh37
NC_000006.10:g.108062615G=	NCBI36
NG_028200.1:g.149606G=
NG_028200.2:g.149606G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1874G= MANE Select	ENSP00000318900.5:p.Arg625=
ENST00000317357.9:c.1874G=	ENSP00000318900.5:p.Arg625=
NM_018013.3:c.1874G=	NP_060483.3:p.Arg625=
XM_005267041.3:c.2027G=	XP_005267098.1:p.Arg676=
XM_005267042.3:c.1931G=	XP_005267099.1:p.Arg644=
XM_011535920.1:c.2027G=	XP_011534222.1:p.Arg676=
XM_011535921.1:c.1913G=	XP_011534223.1:p.Arg638=
XM_011535922.1:c.1286G=	XP_011534224.1:p.Arg429=
XM_011535923.1:c.1097G=	XP_011534225.1:p.Arg366=
XM_005267041.4:c.2027G=	XP_005267098.1:p.Arg676=
XM_005267042.4:c.1931G=	XP_005267099.1:p.Arg644=
XM_011535920.2:c.2027G=	XP_011534222.1:p.Arg676=
XM_011535921.2:c.1913G=	XP_011534223.1:p.Arg638=
XM_011535923.2:c.1097G=	XP_011534225.1:p.Arg366=
XM_017010991.1:c.1427G=	XP_016866480.1:p.Arg476=
XM_017010992.1:c.1427G=	XP_016866481.1:p.Arg476=
XM_017010993.1:c.1427G=	XP_016866482.1:p.Arg476=
XM_017010994.1:c.1427G=	XP_016866483.1:p.Arg476=
NM_018013.4:c.1874G= MANE Select	NP_060483.3:p.Arg625=