Canonical Allele Identifier: CA365171209

Gene: SOBP

Linked Data

• dbSNP Id: rs1554190709
• gnomAD v4: 6-107634591-TC-T
• MyVariant Identifiers: chr6:g.107955796del (hg19) ; chr6:g.107634593del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634597del , CM000668.2:g.107634597del	GRCh38
NC_000006.11:g.107955801del , CM000668.1:g.107955801del	GRCh37
NC_000006.10:g.108062494del	NCBI36
NG_028200.1:g.149485del
NG_028200.2:g.149485del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1753del MANE Select	ENSP00000318900.5:p.Arg585GlyfsTer22
ENST00000317357.9:c.1753del	ENSP00000318900.5:p.Arg585GlyfsTer22
NM_018013.3:c.1753del	NP_060483.3:p.Arg585GlyfsTer22
XM_005267041.3:c.1906del	XP_005267098.1:p.Arg636GlyfsTer22
XM_005267042.3:c.1810del	XP_005267099.1:p.Arg604GlyfsTer22
XM_011535920.1:c.1906del	XP_011534222.1:p.Arg636GlyfsTer22
XM_011535921.1:c.1792del	XP_011534223.1:p.Arg598GlyfsTer22
XM_011535922.1:c.1165del	XP_011534224.1:p.Arg389GlyfsTer22
XM_011535923.1:c.976del	XP_011534225.1:p.Arg326GlyfsTer22
XM_005267041.4:c.1906del	XP_005267098.1:p.Arg636GlyfsTer22
XM_005267042.4:c.1810del	XP_005267099.1:p.Arg604GlyfsTer22
XM_011535920.2:c.1906del	XP_011534222.1:p.Arg636GlyfsTer22
XM_011535921.2:c.1792del	XP_011534223.1:p.Arg598GlyfsTer22
XM_011535923.2:c.976del	XP_011534225.1:p.Arg326GlyfsTer22
XM_017010991.1:c.1306del	XP_016866480.1:p.Arg436GlyfsTer22
XM_017010992.1:c.1306del	XP_016866481.1:p.Arg436GlyfsTer22
XM_017010993.1:c.1306del	XP_016866482.1:p.Arg436GlyfsTer22
XM_017010994.1:c.1306del	XP_016866483.1:p.Arg436GlyfsTer22
NM_018013.4:c.1753del MANE Select	NP_060483.3:p.Arg585GlyfsTer22