Canonical Allele Identifier: CA1653938720

Gene: SOBP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634480G= , CM000668.2:g.107634480G=	GRCh38
NC_000006.11:g.107955684G= , CM000668.1:g.107955684G=	GRCh37
NC_000006.10:g.108062377G=	NCBI36
NG_028200.1:g.149368G=
NG_028200.2:g.149368G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1636G= MANE Select	ENSP00000318900.5:p.Val546=
ENST00000317357.9:c.1636G=	ENSP00000318900.5:p.Val546=
NM_018013.3:c.1636G=	NP_060483.3:p.Val546=
XM_005267041.3:c.1789G=	XP_005267098.1:p.Val597=
XM_005267042.3:c.1693G=	XP_005267099.1:p.Val565=
XM_011535920.1:c.1789G=	XP_011534222.1:p.Val597=
XM_011535921.1:c.1675G=	XP_011534223.1:p.Val559=
XM_011535922.1:c.1048G=	XP_011534224.1:p.Val350=
XM_011535923.1:c.859G=	XP_011534225.1:p.Val287=
XM_005267041.4:c.1789G=	XP_005267098.1:p.Val597=
XM_005267042.4:c.1693G=	XP_005267099.1:p.Val565=
XM_011535920.2:c.1789G=	XP_011534222.1:p.Val597=
XM_011535921.2:c.1675G=	XP_011534223.1:p.Val559=
XM_011535923.2:c.859G=	XP_011534225.1:p.Val287=
XM_017010991.1:c.1189G=	XP_016866480.1:p.Val397=
XM_017010992.1:c.1189G=	XP_016866481.1:p.Val397=
XM_017010993.1:c.1189G=	XP_016866482.1:p.Val397=
XM_017010994.1:c.1189G=	XP_016866483.1:p.Val397=
NM_018013.4:c.1636G= MANE Select	NP_060483.3:p.Val546=