Canonical Allele Identifier: CA1653939128

Gene: SOBP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634704G= , CM000668.2:g.107634704G=	GRCh38
NC_000006.11:g.107955908G= , CM000668.1:g.107955908G=	GRCh37
NC_000006.10:g.108062601G=	NCBI36
NG_028200.1:g.149592G=
NG_028200.2:g.149592G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1860G= MANE Select	ENSP00000318900.5:p.Val620=
ENST00000317357.9:c.1860G=	ENSP00000318900.5:p.Val620=
NM_018013.3:c.1860G=	NP_060483.3:p.Val620=
XM_005267041.3:c.2013G=	XP_005267098.1:p.Val671=
XM_005267042.3:c.1917G=	XP_005267099.1:p.Val639=
XM_011535920.1:c.2013G=	XP_011534222.1:p.Val671=
XM_011535921.1:c.1899G=	XP_011534223.1:p.Val633=
XM_011535922.1:c.1272G=	XP_011534224.1:p.Val424=
XM_011535923.1:c.1083G=	XP_011534225.1:p.Val361=
XM_005267041.4:c.2013G=	XP_005267098.1:p.Val671=
XM_005267042.4:c.1917G=	XP_005267099.1:p.Val639=
XM_011535920.2:c.2013G=	XP_011534222.1:p.Val671=
XM_011535921.2:c.1899G=	XP_011534223.1:p.Val633=
XM_011535923.2:c.1083G=	XP_011534225.1:p.Val361=
XM_017010991.1:c.1413G=	XP_016866480.1:p.Val471=
XM_017010992.1:c.1413G=	XP_016866481.1:p.Val471=
XM_017010993.1:c.1413G=	XP_016866482.1:p.Val471=
XM_017010994.1:c.1413G=	XP_016866483.1:p.Val471=
NM_018013.4:c.1860G= MANE Select	NP_060483.3:p.Val620=