Canonical Allele Identifier: CA1653938650

Gene: SOBP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634458C= , CM000668.2:g.107634458C=	GRCh38
NC_000006.11:g.107955662C= , CM000668.1:g.107955662C=	GRCh37
NC_000006.10:g.108062355C=	NCBI36
NG_028200.1:g.149346C=
NG_028200.2:g.149346C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1614C= MANE Select	ENSP00000318900.5:p.Pro538=
ENST00000317357.9:c.1614C=	ENSP00000318900.5:p.Pro538=
NM_018013.3:c.1614C=	NP_060483.3:p.Pro538=
XM_005267041.3:c.1767C=	XP_005267098.1:p.Pro589=
XM_005267042.3:c.1671C=	XP_005267099.1:p.Pro557=
XM_011535920.1:c.1767C=	XP_011534222.1:p.Pro589=
XM_011535921.1:c.1653C=	XP_011534223.1:p.Pro551=
XM_011535922.1:c.1026C=	XP_011534224.1:p.Pro342=
XM_011535923.1:c.837C=	XP_011534225.1:p.Pro279=
XM_005267041.4:c.1767C=	XP_005267098.1:p.Pro589=
XM_005267042.4:c.1671C=	XP_005267099.1:p.Pro557=
XM_011535920.2:c.1767C=	XP_011534222.1:p.Pro589=
XM_011535921.2:c.1653C=	XP_011534223.1:p.Pro551=
XM_011535923.2:c.837C=	XP_011534225.1:p.Pro279=
XM_017010991.1:c.1167C=	XP_016866480.1:p.Pro389=
XM_017010992.1:c.1167C=	XP_016866481.1:p.Pro389=
XM_017010993.1:c.1167C=	XP_016866482.1:p.Pro389=
XM_017010994.1:c.1167C=	XP_016866483.1:p.Pro389=
NM_018013.4:c.1614C= MANE Select	NP_060483.3:p.Pro538=