Canonical Allele Identifier: CA1653939280

Gene: SOBP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634767C= , CM000668.2:g.107634767C=	GRCh38
NC_000006.11:g.107955971C= , CM000668.1:g.107955971C=	GRCh37
NC_000006.10:g.108062664C=	NCBI36
NG_028200.1:g.149655C=
NG_028200.2:g.149655C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1923C= MANE Select	ENSP00000318900.5:p.Gly641=
ENST00000317357.9:c.1923C=	ENSP00000318900.5:p.Gly641=
NM_018013.3:c.1923C=	NP_060483.3:p.Gly641=
XM_005267041.3:c.2076C=	XP_005267098.1:p.Gly692=
XM_005267042.3:c.1980C=	XP_005267099.1:p.Gly660=
XM_011535920.1:c.2076C=	XP_011534222.1:p.Gly692=
XM_011535921.1:c.1962C=	XP_011534223.1:p.Gly654=
XM_011535922.1:c.1335C=	XP_011534224.1:p.Gly445=
XM_011535923.1:c.1146C=	XP_011534225.1:p.Gly382=
XM_005267041.4:c.2076C=	XP_005267098.1:p.Gly692=
XM_005267042.4:c.1980C=	XP_005267099.1:p.Gly660=
XM_011535920.2:c.2076C=	XP_011534222.1:p.Gly692=
XM_011535921.2:c.1962C=	XP_011534223.1:p.Gly654=
XM_011535923.2:c.1146C=	XP_011534225.1:p.Gly382=
XM_017010991.1:c.1476C=	XP_016866480.1:p.Gly492=
XM_017010992.1:c.1476C=	XP_016866481.1:p.Gly492=
XM_017010993.1:c.1476C=	XP_016866482.1:p.Gly492=
XM_017010994.1:c.1476C=	XP_016866483.1:p.Gly492=
NM_018013.4:c.1923C= MANE Select	NP_060483.3:p.Gly641=