Canonical Allele Identifier: CA2679876748

Gene: SOBP

Linked Data

• gnomAD v4: 6-107634668-G-GGCGCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634669_107634674dup , CM000668.2:g.107634669_107634674dup	GRCh38
NC_000006.11:g.107955873_107955878dup , CM000668.1:g.107955873_107955878dup	GRCh37
NC_000006.10:g.108062566_108062571dup	NCBI36
NG_028200.1:g.149557_149562dup
NG_028200.2:g.149557_149562dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1825_1830dup MANE Select	ENSP00000318900.5:p.Pro610_Thr611insAlaPro
ENST00000317357.9:c.1825_1830dup	ENSP00000318900.5:p.Pro610_Thr611insAlaPro
NM_018013.3:c.1825_1830dup	NP_060483.3:p.Pro610_Thr611insAlaPro
XM_005267041.3:c.1978_1983dup	XP_005267098.1:p.Pro661_Thr662insAlaPro
XM_005267042.3:c.1882_1887dup	XP_005267099.1:p.Pro629_Thr630insAlaPro
XM_011535920.1:c.1978_1983dup	XP_011534222.1:p.Pro661_Thr662insAlaPro
XM_011535921.1:c.1864_1869dup	XP_011534223.1:p.Pro623_Thr624insAlaPro
XM_011535922.1:c.1237_1242dup	XP_011534224.1:p.Pro414_Thr415insAlaPro
XM_011535923.1:c.1048_1053dup	XP_011534225.1:p.Pro351_Thr352insAlaPro
XM_005267041.4:c.1978_1983dup	XP_005267098.1:p.Pro661_Thr662insAlaPro
XM_005267042.4:c.1882_1887dup	XP_005267099.1:p.Pro629_Thr630insAlaPro
XM_011535920.2:c.1978_1983dup	XP_011534222.1:p.Pro661_Thr662insAlaPro
XM_011535921.2:c.1864_1869dup	XP_011534223.1:p.Pro623_Thr624insAlaPro
XM_011535923.2:c.1048_1053dup	XP_011534225.1:p.Pro351_Thr352insAlaPro
XM_017010991.1:c.1378_1383dup	XP_016866480.1:p.Pro461_Thr462insAlaPro
XM_017010992.1:c.1378_1383dup	XP_016866481.1:p.Pro461_Thr462insAlaPro
XM_017010993.1:c.1378_1383dup	XP_016866482.1:p.Pro461_Thr462insAlaPro
XM_017010994.1:c.1378_1383dup	XP_016866483.1:p.Pro461_Thr462insAlaPro
NM_018013.4:c.1825_1830dup MANE Select	NP_060483.3:p.Pro610_Thr611insAlaPro