Canonical Allele Identifier: CA1653938623

Gene: SOBP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634449_107634461delinsGCCCATCCCCATC , CM000668.2:g.107634449_107634461delinsGCCCATCCCCATC	GRCh38
NC_000006.11:g.107955653_107955665delinsGCCCATCCCCATC , CM000668.1:g.107955653_107955665delinsGCCCATCCCCATC	GRCh37
NC_000006.10:g.108062346_108062358delinsGCCCATCCCCATC	NCBI36
NG_028200.1:g.149337_149349delinsGCCCATCCCCATC
NG_028200.2:g.149337_149349delinsGCCCATCCCCATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1605_1617delinsGCCCATCCCCATC MANE Select	ENSP00000318900.5:p.Val535=
ENST00000317357.9:c.1605_1617delinsGCCCATCCCCATC	ENSP00000318900.5:p.Val535=
NM_018013.3:c.1605_1617delinsGCCCATCCCCATC	NP_060483.3:p.Val535=
XM_005267041.3:c.1758_1770delinsGCCCATCCCCATC	XP_005267098.1:p.Val586=
XM_005267042.3:c.1662_1674delinsGCCCATCCCCATC	XP_005267099.1:p.Val554=
XM_011535920.1:c.1758_1770delinsGCCCATCCCCATC	XP_011534222.1:p.Val586=
XM_011535921.1:c.1644_1656delinsGCCCATCCCCATC	XP_011534223.1:p.Val548=
XM_011535922.1:c.1017_1029delinsGCCCATCCCCATC	XP_011534224.1:p.Val339=
XM_011535923.1:c.828_840delinsGCCCATCCCCATC	XP_011534225.1:p.Val276=
XM_005267041.4:c.1758_1770delinsGCCCATCCCCATC	XP_005267098.1:p.Val586=
XM_005267042.4:c.1662_1674delinsGCCCATCCCCATC	XP_005267099.1:p.Val554=
XM_011535920.2:c.1758_1770delinsGCCCATCCCCATC	XP_011534222.1:p.Val586=
XM_011535921.2:c.1644_1656delinsGCCCATCCCCATC	XP_011534223.1:p.Val548=
XM_011535923.2:c.828_840delinsGCCCATCCCCATC	XP_011534225.1:p.Val276=
XM_017010991.1:c.1158_1170delinsGCCCATCCCCATC	XP_016866480.1:p.Val386=
XM_017010992.1:c.1158_1170delinsGCCCATCCCCATC	XP_016866481.1:p.Val386=
XM_017010993.1:c.1158_1170delinsGCCCATCCCCATC	XP_016866482.1:p.Val386=
XM_017010994.1:c.1158_1170delinsGCCCATCCCCATC	XP_016866483.1:p.Val386=
NM_018013.4:c.1605_1617delinsGCCCATCCCCATC MANE Select	NP_060483.3:p.Val535=