Canonical Allele Identifier: CA1653938692

Gene: SOBP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634471A= , CM000668.2:g.107634471A=	GRCh38
NC_000006.11:g.107955675A= , CM000668.1:g.107955675A=	GRCh37
NC_000006.10:g.108062368A=	NCBI36
NG_028200.1:g.149359A=
NG_028200.2:g.149359A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1627A= MANE Select	ENSP00000318900.5:p.Ile543=
ENST00000317357.9:c.1627A=	ENSP00000318900.5:p.Ile543=
NM_018013.3:c.1627A=	NP_060483.3:p.Ile543=
XM_005267041.3:c.1780A=	XP_005267098.1:p.Ile594=
XM_005267042.3:c.1684A=	XP_005267099.1:p.Ile562=
XM_011535920.1:c.1780A=	XP_011534222.1:p.Ile594=
XM_011535921.1:c.1666A=	XP_011534223.1:p.Ile556=
XM_011535922.1:c.1039A=	XP_011534224.1:p.Ile347=
XM_011535923.1:c.850A=	XP_011534225.1:p.Ile284=
XM_005267041.4:c.1780A=	XP_005267098.1:p.Ile594=
XM_005267042.4:c.1684A=	XP_005267099.1:p.Ile562=
XM_011535920.2:c.1780A=	XP_011534222.1:p.Ile594=
XM_011535921.2:c.1666A=	XP_011534223.1:p.Ile556=
XM_011535923.2:c.850A=	XP_011534225.1:p.Ile284=
XM_017010991.1:c.1180A=	XP_016866480.1:p.Ile394=
XM_017010992.1:c.1180A=	XP_016866481.1:p.Ile394=
XM_017010993.1:c.1180A=	XP_016866482.1:p.Ile394=
XM_017010994.1:c.1180A=	XP_016866483.1:p.Ile394=
NM_018013.4:c.1627A= MANE Select	NP_060483.3:p.Ile543=