Canonical Allele Identifier: CA2679876746

Gene: SOBP

Linked Data

• gnomAD v4: 6-107634656-GGCCCTGAGCCTGGCGCCCACGCCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107634660_107634683del , CM000668.2:g.107634660_107634683del	GRCh38
NC_000006.11:g.107955864_107955887del , CM000668.1:g.107955864_107955887del	GRCh37
NC_000006.10:g.108062557_108062580del	NCBI36
NG_028200.1:g.149548_149571del
NG_028200.2:g.149548_149571del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317357.10:c.1816_1839del MANE Select	ENSP00000318900.5:p.Leu606_Ala613del
ENST00000317357.9:c.1816_1839del	ENSP00000318900.5:p.Leu606_Ala613del
NM_018013.3:c.1816_1839del	NP_060483.3:p.Leu606_Ala613del
XM_005267041.3:c.1969_1992del	XP_005267098.1:p.Leu657_Ala664del
XM_005267042.3:c.1873_1896del	XP_005267099.1:p.Leu625_Ala632del
XM_011535920.1:c.1969_1992del	XP_011534222.1:p.Leu657_Ala664del
XM_011535921.1:c.1855_1878del	XP_011534223.1:p.Leu619_Ala626del
XM_011535922.1:c.1228_1251del	XP_011534224.1:p.Leu410_Ala417del
XM_011535923.1:c.1039_1062del	XP_011534225.1:p.Leu347_Ala354del
XM_005267041.4:c.1969_1992del	XP_005267098.1:p.Leu657_Ala664del
XM_005267042.4:c.1873_1896del	XP_005267099.1:p.Leu625_Ala632del
XM_011535920.2:c.1969_1992del	XP_011534222.1:p.Leu657_Ala664del
XM_011535921.2:c.1855_1878del	XP_011534223.1:p.Leu619_Ala626del
XM_011535923.2:c.1039_1062del	XP_011534225.1:p.Leu347_Ala354del
XM_017010991.1:c.1369_1392del	XP_016866480.1:p.Leu457_Ala464del
XM_017010992.1:c.1369_1392del	XP_016866481.1:p.Leu457_Ala464del
XM_017010993.1:c.1369_1392del	XP_016866482.1:p.Leu457_Ala464del
XM_017010994.1:c.1369_1392del	XP_016866483.1:p.Leu457_Ala464del
NM_018013.4:c.1816_1839del MANE Select	NP_060483.3:p.Leu606_Ala613del