Canonical Allele Identifier: CA2679876772

Gene: SOBP

Linked Data

• gnomAD v4: 6-107634889-C-CGGGCGCCGCG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634890_107634891insGGCGCCGCGG , CM000668.2:g.107634890_107634891insGGCGCCGCGG	GRCh38
NC_000006.11:g.107956094_107956095insGGCGCCGCGG , CM000668.1:g.107956094_107956095insGGCGCCGCGG	GRCh37
NC_000006.10:g.108062787_108062788insGGCGCCGCGG	NCBI36
NG_028200.1:g.149778_149779insGGCGCCGCGG
NG_028200.2:g.149778_149779insGGCGCCGCGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.2046_2047insGGCGCCGCGG MANE Select	ENSP00000318900.5:p.Ser683GlyfsTer?
ENST00000317357.9:c.2046_2047insGGCGCCGCGG	ENSP00000318900.5:p.Ser683GlyfsTer?
NM_018013.3:c.2046_2047insGGCGCCGCGG	NP_060483.3:p.Ser683GlyfsTer?
XM_005267041.3:c.2199_2200insGGCGCCGCGG	XP_005267098.1:p.Ser734GlyfsTer?
XM_005267042.3:c.2103_2104insGGCGCCGCGG	XP_005267099.1:p.Ser702GlyfsTer?
XM_011535920.1:c.2199_2200insGGCGCCGCGG	XP_011534222.1:p.Ser734GlyfsTer?
XM_011535921.1:c.2085_2086insGGCGCCGCGG	XP_011534223.1:p.Ser696GlyfsTer?
XM_011535922.1:c.1458_1459insGGCGCCGCGG	XP_011534224.1:p.Ser487GlyfsTer?
XM_011535923.1:c.1269_1270insGGCGCCGCGG	XP_011534225.1:p.Ser424GlyfsTer?
XM_005267041.4:c.2199_2200insGGCGCCGCGG	XP_005267098.1:p.Ser734GlyfsTer?
XM_005267042.4:c.2103_2104insGGCGCCGCGG	XP_005267099.1:p.Ser702GlyfsTer?
XM_011535920.2:c.2199_2200insGGCGCCGCGG	XP_011534222.1:p.Ser734GlyfsTer?
XM_011535921.2:c.2085_2086insGGCGCCGCGG	XP_011534223.1:p.Ser696GlyfsTer?
XM_011535923.2:c.1269_1270insGGCGCCGCGG	XP_011534225.1:p.Ser424GlyfsTer?
XM_017010991.1:c.1599_1600insGGCGCCGCGG	XP_016866480.1:p.Ser534GlyfsTer?
XM_017010992.1:c.1599_1600insGGCGCCGCGG	XP_016866481.1:p.Ser534GlyfsTer?
XM_017010993.1:c.1599_1600insGGCGCCGCGG	XP_016866482.1:p.Ser534GlyfsTer?
XM_017010994.1:c.1599_1600insGGCGCCGCGG	XP_016866483.1:p.Ser534GlyfsTer?
NM_018013.4:c.2046_2047insGGCGCCGCGG MANE Select	NP_060483.3:p.Ser683GlyfsTer?