Canonical Allele Identifier: CA451581676

Gene: SOBP

Linked Data

• MyVariant Identifiers: chr6:g.107955680T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634476T>A , CM000668.2:g.107634476T>A	GRCh38
NC_000006.11:g.107955680T>A , CM000668.1:g.107955680T>A	GRCh37
NC_000006.10:g.108062373T>A	NCBI36
NG_028200.1:g.149364T>A
NG_028200.2:g.149364T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1632T>A MANE Select	ENSP00000318900.5:p.Pro544=
ENST00000317357.9:c.1632T>A	ENSP00000318900.5:p.Pro544=
NM_018013.3:c.1632T>A	NP_060483.3:p.Pro544=
XM_005267041.3:c.1785T>A	XP_005267098.1:p.Pro595=
XM_005267042.3:c.1689T>A	XP_005267099.1:p.Pro563=
XM_011535920.1:c.1785T>A	XP_011534222.1:p.Pro595=
XM_011535921.1:c.1671T>A	XP_011534223.1:p.Pro557=
XM_011535922.1:c.1044T>A	XP_011534224.1:p.Pro348=
XM_011535923.1:c.855T>A	XP_011534225.1:p.Pro285=
XM_005267041.4:c.1785T>A	XP_005267098.1:p.Pro595=
XM_005267042.4:c.1689T>A	XP_005267099.1:p.Pro563=
XM_011535920.2:c.1785T>A	XP_011534222.1:p.Pro595=
XM_011535921.2:c.1671T>A	XP_011534223.1:p.Pro557=
XM_011535923.2:c.855T>A	XP_011534225.1:p.Pro285=
XM_017010991.1:c.1185T>A	XP_016866480.1:p.Pro395=
XM_017010992.1:c.1185T>A	XP_016866481.1:p.Pro395=
XM_017010993.1:c.1185T>A	XP_016866482.1:p.Pro395=
XM_017010994.1:c.1185T>A	XP_016866483.1:p.Pro395=
NM_018013.4:c.1632T>A MANE Select	NP_060483.3:p.Pro544=