Canonical Allele Identifier: CA2772523132

Gene: SOBP

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634889del , CM000668.2:g.107634889del	GRCh38
NC_000006.11:g.107956093del , CM000668.1:g.107956093del	GRCh37
NC_000006.10:g.108062786del	NCBI36
NG_028200.1:g.149777del
NG_028200.2:g.149777del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.2045del MANE Select	ENSP00000318900.5:p.Pro682ArgfsTer?
ENST00000317357.9:c.2045del	ENSP00000318900.5:p.Pro682ArgfsTer?
NM_018013.3:c.2045del	NP_060483.3:p.Pro682ArgfsTer?
XM_005267041.3:c.2198del	XP_005267098.1:p.Pro733ArgfsTer?
XM_005267042.3:c.2102del	XP_005267099.1:p.Pro701ArgfsTer?
XM_011535920.1:c.2198del	XP_011534222.1:p.Pro733ArgfsTer?
XM_011535921.1:c.2084del	XP_011534223.1:p.Pro695ArgfsTer?
XM_011535922.1:c.1457del	XP_011534224.1:p.Pro486ArgfsTer?
XM_011535923.1:c.1268del	XP_011534225.1:p.Pro423ArgfsTer?
XM_005267041.4:c.2198del	XP_005267098.1:p.Pro733ArgfsTer?
XM_005267042.4:c.2102del	XP_005267099.1:p.Pro701ArgfsTer?
XM_011535920.2:c.2198del	XP_011534222.1:p.Pro733ArgfsTer?
XM_011535921.2:c.2084del	XP_011534223.1:p.Pro695ArgfsTer?
XM_011535923.2:c.1268del	XP_011534225.1:p.Pro423ArgfsTer?
XM_017010991.1:c.1598del	XP_016866480.1:p.Pro533ArgfsTer?
XM_017010992.1:c.1598del	XP_016866481.1:p.Pro533ArgfsTer?
XM_017010993.1:c.1598del	XP_016866482.1:p.Pro533ArgfsTer?
XM_017010994.1:c.1598del	XP_016866483.1:p.Pro533ArgfsTer?
NM_018013.4:c.2045del MANE Select	NP_060483.3:p.Pro682ArgfsTer?