Canonical Allele Identifier: CA816903837

Gene: SOBP

Linked Data

• dbSNP Id: rs771892919
• gnomAD v3: 6-107634449-G-GCCCATT
• gnomAD v4: 6-107634449-G-GCCCATT
• MyVariant Identifiers: chr6:g.107955653_107955654insCCCATT (hg19) ; chr6:g.107634449_107634450insCCCATT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634454_107634455insTCCCAT , CM000668.2:g.107634454_107634455insTCCCAT	GRCh38
NC_000006.11:g.107955658_107955659insTCCCAT , CM000668.1:g.107955658_107955659insTCCCAT	GRCh37
NC_000006.10:g.108062351_108062352insTCCCAT	NCBI36
NG_028200.1:g.149342_149343insTCCCAT
NG_028200.2:g.149342_149343insTCCCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1610_1611insTCCCAT MANE Select	ENSP00000318900.5:p.Ile537_Pro538insProIle
ENST00000317357.9:c.1610_1611insTCCCAT	ENSP00000318900.5:p.Ile537_Pro538insProIle
NM_018013.3:c.1610_1611insTCCCAT	NP_060483.3:p.Ile537_Pro538insProIle
XM_005267041.3:c.1763_1764insTCCCAT	XP_005267098.1:p.Ile588_Pro589insProIle
XM_005267042.3:c.1667_1668insTCCCAT	XP_005267099.1:p.Ile556_Pro557insProIle
XM_011535920.1:c.1763_1764insTCCCAT	XP_011534222.1:p.Ile588_Pro589insProIle
XM_011535921.1:c.1649_1650insTCCCAT	XP_011534223.1:p.Ile550_Pro551insProIle
XM_011535922.1:c.1022_1023insTCCCAT	XP_011534224.1:p.Ile341_Pro342insProIle
XM_011535923.1:c.833_834insTCCCAT	XP_011534225.1:p.Ile278_Pro279insProIle
XM_005267041.4:c.1763_1764insTCCCAT	XP_005267098.1:p.Ile588_Pro589insProIle
XM_005267042.4:c.1667_1668insTCCCAT	XP_005267099.1:p.Ile556_Pro557insProIle
XM_011535920.2:c.1763_1764insTCCCAT	XP_011534222.1:p.Ile588_Pro589insProIle
XM_011535921.2:c.1649_1650insTCCCAT	XP_011534223.1:p.Ile550_Pro551insProIle
XM_011535923.2:c.833_834insTCCCAT	XP_011534225.1:p.Ile278_Pro279insProIle
XM_017010991.1:c.1163_1164insTCCCAT	XP_016866480.1:p.Ile388_Pro389insProIle
XM_017010992.1:c.1163_1164insTCCCAT	XP_016866481.1:p.Ile388_Pro389insProIle
XM_017010993.1:c.1163_1164insTCCCAT	XP_016866482.1:p.Ile388_Pro389insProIle
XM_017010994.1:c.1163_1164insTCCCAT	XP_016866483.1:p.Ile388_Pro389insProIle
NM_018013.4:c.1610_1611insTCCCAT MANE Select	NP_060483.3:p.Ile537_Pro538insProIle