Canonical Allele Identifier: CA2739289923

Gene: SOBP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634471_107634476dup , CM000668.2:g.107634471_107634476dup	GRCh38
NC_000006.11:g.107955675_107955680dup , CM000668.1:g.107955675_107955680dup	GRCh37
NC_000006.10:g.108062368_108062373dup	NCBI36
NG_028200.1:g.149359_149364dup
NG_028200.2:g.149359_149364dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1627_1632dup MANE Select	ENSP00000318900.5:p.Pro544_His545insIlePro
ENST00000317357.9:c.1627_1632dup	ENSP00000318900.5:p.Pro544_His545insIlePro
NM_018013.3:c.1627_1632dup	NP_060483.3:p.Pro544_His545insIlePro
XM_005267041.3:c.1780_1785dup	XP_005267098.1:p.Pro595_His596insIlePro
XM_005267042.3:c.1684_1689dup	XP_005267099.1:p.Pro563_His564insIlePro
XM_011535920.1:c.1780_1785dup	XP_011534222.1:p.Pro595_His596insIlePro
XM_011535921.1:c.1666_1671dup	XP_011534223.1:p.Pro557_His558insIlePro
XM_011535922.1:c.1039_1044dup	XP_011534224.1:p.Pro348_His349insIlePro
XM_011535923.1:c.850_855dup	XP_011534225.1:p.Pro285_His286insIlePro
XM_005267041.4:c.1780_1785dup	XP_005267098.1:p.Pro595_His596insIlePro
XM_005267042.4:c.1684_1689dup	XP_005267099.1:p.Pro563_His564insIlePro
XM_011535920.2:c.1780_1785dup	XP_011534222.1:p.Pro595_His596insIlePro
XM_011535921.2:c.1666_1671dup	XP_011534223.1:p.Pro557_His558insIlePro
XM_011535923.2:c.850_855dup	XP_011534225.1:p.Pro285_His286insIlePro
XM_017010991.1:c.1180_1185dup	XP_016866480.1:p.Pro395_His396insIlePro
XM_017010992.1:c.1180_1185dup	XP_016866481.1:p.Pro395_His396insIlePro
XM_017010993.1:c.1180_1185dup	XP_016866482.1:p.Pro395_His396insIlePro
XM_017010994.1:c.1180_1185dup	XP_016866483.1:p.Pro395_His396insIlePro
NM_018013.4:c.1627_1632dup MANE Select	NP_060483.3:p.Pro544_His545insIlePro