Canonical Allele Identifier: CA3946608

Gene: SOBP

Linked Data

• dbSNP Id: rs746750430
• ExAC: 6:107955933 AGCCCCCCGG / A
• gnomAD v2: 6-107955933-AGCCCCCCGG-A
• gnomAD v3: 6-107634729-AGCCCCCCGG-A
• gnomAD v4: 6-107634729-AGCCCCCCGG-A
• MyVariant Identifiers: chr6:g.107955934_107955942del (hg19) ; chr6:g.107634730_107634738del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634741_107634749del , CM000668.2:g.107634741_107634749del	GRCh38
NC_000006.11:g.107955945_107955953del , CM000668.1:g.107955945_107955953del	GRCh37
NC_000006.10:g.108062638_108062646del	NCBI36
NG_028200.1:g.149629_149637del
NG_028200.2:g.149629_149637del

Transcript Alleles

HGVS	Amino-acid change
ENST00000317357.10:c.1897_1905del MANE Select	ENSP00000318900.5:p.Pro633_Gly635del
ENST00000317357.9:c.1897_1905del	ENSP00000318900.5:p.Pro633_Gly635del
NM_018013.3:c.1897_1905del	NP_060483.3:p.Pro633_Gly635del
XM_005267041.3:c.2050_2058del	XP_005267098.1:p.Pro684_Gly686del
XM_005267042.3:c.1954_1962del	XP_005267099.1:p.Pro652_Gly654del
XM_011535920.1:c.2050_2058del	XP_011534222.1:p.Pro684_Gly686del
XM_011535921.1:c.1936_1944del	XP_011534223.1:p.Pro646_Gly648del
XM_011535922.1:c.1309_1317del	XP_011534224.1:p.Pro437_Gly439del
XM_011535923.1:c.1120_1128del	XP_011534225.1:p.Pro374_Gly376del
XM_005267041.4:c.2050_2058del	XP_005267098.1:p.Pro684_Gly686del
XM_005267042.4:c.1954_1962del	XP_005267099.1:p.Pro652_Gly654del
XM_011535920.2:c.2050_2058del	XP_011534222.1:p.Pro684_Gly686del
XM_011535921.2:c.1936_1944del	XP_011534223.1:p.Pro646_Gly648del
XM_011535923.2:c.1120_1128del	XP_011534225.1:p.Pro374_Gly376del
XM_017010991.1:c.1450_1458del	XP_016866480.1:p.Pro484_Gly486del
XM_017010992.1:c.1450_1458del	XP_016866481.1:p.Pro484_Gly486del
XM_017010993.1:c.1450_1458del	XP_016866482.1:p.Pro484_Gly486del
XM_017010994.1:c.1450_1458del	XP_016866483.1:p.Pro484_Gly486del
NM_018013.4:c.1897_1905del MANE Select	NP_060483.3:p.Pro633_Gly635del