Canonical Allele Identifier: CA1786790582

Gene: FAM110B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.58073991_58074007delinsGTCCTGCGGTCAGGAAA , CM000670.2:g.58073991_58074007delinsGTCCTGCGGTCAGGAAA	GRCh38
NC_000008.10:g.58986550_58986566delinsGTCCTGCGGTCAGGAAA , CM000670.1:g.58986550_58986566delinsGTCCTGCGGTCAGGAAA	GRCh37
NC_000008.9:g.59149104_59149120delinsGTCCTGCGGTCAGGAAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519262.6:c.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA MANE Select	ENSP00000509301.1:n.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAA...
ENST00000361488.7:c.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA	ENSP00000355204.3:n.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAA...
ENST00000518427.5:n.182-1544_182-1528delinsGTCCTGCGGTCAGGAAA
ENST00000519262.5:n.397-1544_397-1528delinsGTCCTGCGGTCAGGAAA
ENST00000520369.5:n.338-1544_338-1528delinsGTCCTGCGGTCAGGAAA
ENST00000521413.1:n.46-1544_46-1528delinsGTCCTGCGGTCAGGAAA
ENST00000522059.5:n.89-1544_89-1528delinsGTCCTGCGGTCAGGAAA
ENST00000523486.5:n.137-1544_137-1528delinsGTCCTGCGGTCAGGAAA
NM_147189.2:c.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA	NP_671722.1:n.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA
XM_005251324.1:c.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA	XP_005251381.1:n.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA
XM_005251325.2:c.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA	XP_005251382.1:n.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA
XM_005251326.1:c.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA	XP_005251383.1:n.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA
XM_005251324.3:c.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA	XP_005251381.1:n.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA
XM_005251325.3:c.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA	XP_005251382.1:n.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA
XM_005251326.3:c.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA	XP_005251383.1:n.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA
XM_017013948.1:c.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA	XP_016869437.1:n.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA
NM_147189.3:c.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA	NP_671722.1:n.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA
NM_001377989.1:c.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA MANE Select	NP_001364918.1:n.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA
NM_001377997.1:c.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA	NP_001364926.1:n.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA
NM_001377998.1:c.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA	NP_001364927.1:n.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA
NM_147189.4:c.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA	NP_671722.1:n.-413-1544_-413-1528delinsGTCCTGCGGTCAGGAAA