Canonical Allele Identifier: CA1653939309

Gene: SOBP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634791G= , CM000668.2:g.107634791G=	GRCh38
NC_000006.11:g.107955995G= , CM000668.1:g.107955995G=	GRCh37
NC_000006.10:g.108062688G=	NCBI36
NG_028200.1:g.149679G=
NG_028200.2:g.149679G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1947G= MANE Select	ENSP00000318900.5:p.Pro649=
ENST00000317357.9:c.1947G=	ENSP00000318900.5:p.Pro649=
NM_018013.3:c.1947G=	NP_060483.3:p.Pro649=
XM_005267041.3:c.2100G=	XP_005267098.1:p.Pro700=
XM_005267042.3:c.2004G=	XP_005267099.1:p.Pro668=
XM_011535920.1:c.2100G=	XP_011534222.1:p.Pro700=
XM_011535921.1:c.1986G=	XP_011534223.1:p.Pro662=
XM_011535922.1:c.1359G=	XP_011534224.1:p.Pro453=
XM_011535923.1:c.1170G=	XP_011534225.1:p.Pro390=
XM_005267041.4:c.2100G=	XP_005267098.1:p.Pro700=
XM_005267042.4:c.2004G=	XP_005267099.1:p.Pro668=
XM_011535920.2:c.2100G=	XP_011534222.1:p.Pro700=
XM_011535921.2:c.1986G=	XP_011534223.1:p.Pro662=
XM_011535923.2:c.1170G=	XP_011534225.1:p.Pro390=
XM_017010991.1:c.1500G=	XP_016866480.1:p.Pro500=
XM_017010992.1:c.1500G=	XP_016866481.1:p.Pro500=
XM_017010993.1:c.1500G=	XP_016866482.1:p.Pro500=
XM_017010994.1:c.1500G=	XP_016866483.1:p.Pro500=
NM_018013.4:c.1947G= MANE Select	NP_060483.3:p.Pro649=