Canonical Allele Identifier: CA1653939135

Gene: SOBP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634707G= , CM000668.2:g.107634707G=	GRCh38
NC_000006.11:g.107955911G= , CM000668.1:g.107955911G=	GRCh37
NC_000006.10:g.108062604G=	NCBI36
NG_028200.1:g.149595G=
NG_028200.2:g.149595G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1863G= MANE Select	ENSP00000318900.5:p.Val621=
ENST00000317357.9:c.1863G=	ENSP00000318900.5:p.Val621=
NM_018013.3:c.1863G=	NP_060483.3:p.Val621=
XM_005267041.3:c.2016G=	XP_005267098.1:p.Val672=
XM_005267042.3:c.1920G=	XP_005267099.1:p.Val640=
XM_011535920.1:c.2016G=	XP_011534222.1:p.Val672=
XM_011535921.1:c.1902G=	XP_011534223.1:p.Val634=
XM_011535922.1:c.1275G=	XP_011534224.1:p.Val425=
XM_011535923.1:c.1086G=	XP_011534225.1:p.Val362=
XM_005267041.4:c.2016G=	XP_005267098.1:p.Val672=
XM_005267042.4:c.1920G=	XP_005267099.1:p.Val640=
XM_011535920.2:c.2016G=	XP_011534222.1:p.Val672=
XM_011535921.2:c.1902G=	XP_011534223.1:p.Val634=
XM_011535923.2:c.1086G=	XP_011534225.1:p.Val362=
XM_017010991.1:c.1416G=	XP_016866480.1:p.Val472=
XM_017010992.1:c.1416G=	XP_016866481.1:p.Val472=
XM_017010993.1:c.1416G=	XP_016866482.1:p.Val472=
XM_017010994.1:c.1416G=	XP_016866483.1:p.Val472=
NM_018013.4:c.1863G= MANE Select	NP_060483.3:p.Val621=