Canonical Allele Identifier: CA917829048

Gene: SOBP

Linked Data

• dbSNP Id: rs1583295897
• gnomAD v4: 6-107634739-GCCCCCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634740_107634745del , CM000668.2:g.107634740_107634745del	GRCh38
NC_000006.11:g.107955944_107955949del , CM000668.1:g.107955944_107955949del	GRCh37
NC_000006.10:g.108062637_108062642del	NCBI36
NG_028200.1:g.149628_149633del
NG_028200.2:g.149628_149633del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1896_1901del MANE Select	ENSP00000318900.5:p.Pro633_Pro634del
ENST00000317357.9:c.1896_1901del	ENSP00000318900.5:p.Pro633_Pro634del
NM_018013.3:c.1896_1901del	NP_060483.3:p.Pro633_Pro634del
XM_005267041.3:c.2049_2054del	XP_005267098.1:p.Pro684_Pro685del
XM_005267042.3:c.1953_1958del	XP_005267099.1:p.Pro652_Pro653del
XM_011535920.1:c.2049_2054del	XP_011534222.1:p.Pro684_Pro685del
XM_011535921.1:c.1935_1940del	XP_011534223.1:p.Pro646_Pro647del
XM_011535922.1:c.1308_1313del	XP_011534224.1:p.Pro437_Pro438del
XM_011535923.1:c.1119_1124del	XP_011534225.1:p.Pro374_Pro375del
XM_005267041.4:c.2049_2054del	XP_005267098.1:p.Pro684_Pro685del
XM_005267042.4:c.1953_1958del	XP_005267099.1:p.Pro652_Pro653del
XM_011535920.2:c.2049_2054del	XP_011534222.1:p.Pro684_Pro685del
XM_011535921.2:c.1935_1940del	XP_011534223.1:p.Pro646_Pro647del
XM_011535923.2:c.1119_1124del	XP_011534225.1:p.Pro374_Pro375del
XM_017010991.1:c.1449_1454del	XP_016866480.1:p.Pro484_Pro485del
XM_017010992.1:c.1449_1454del	XP_016866481.1:p.Pro484_Pro485del
XM_017010993.1:c.1449_1454del	XP_016866482.1:p.Pro484_Pro485del
XM_017010994.1:c.1449_1454del	XP_016866483.1:p.Pro484_Pro485del
NM_018013.4:c.1896_1901del MANE Select	NP_060483.3:p.Pro633_Pro634del