Canonical Allele Identifier: CA1114252741
Gene: FAM110B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.58073808_58073809insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG , CM000670.2:g.58073808_58073809insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG GRCh38
NC_000008.10:g.58986367_58986368insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG , CM000670.1:g.58986367_58986368insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG GRCh37
NC_000008.9:g.59148921_59148922insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000519262.6:c.-413-1727_-413-1726insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG MANE Select ENSP00000509301.1:n.-413-1727_-413-1726in...
ENST00000361488.7:c.-413-1727_-413-1726insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG ENSP00000355204.3:n.-413-1727_-413-1726in...
ENST00000518427.5:n.182-1727_182-1726insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG
ENST00000519262.5:n.397-1727_397-1726insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG
ENST00000520369.5:n.338-1727_338-1726insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG
ENST00000521413.1:n.46-1727_46-1726insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG
ENST00000522059.5:n.89-1727_89-1726insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG
ENST00000523486.5:n.137-1727_137-1726insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG
NM_147189.2:c.-413-1727_-413-1726insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG NP_671722.1:n.-413-1727_-413-1726insCTTTA...
XM_005251324.1:c.-413-1727_-413-1726insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG XP_005251381.1:n.-413-1727_-413-1726insCT...
XM_005251325.2:c.-413-1727_-413-1726insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG XP_005251382.1:n.-413-1727_-413-1726insCT...
XM_005251326.1:c.-413-1727_-413-1726insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG XP_005251383.1:n.-413-1727_-413-1726insCT...
XM_005251324.3:c.-413-1727_-413-1726insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG XP_005251381.1:n.-413-1727_-413-1726insCT...
XM_005251325.3:c.-413-1727_-413-1726insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG XP_005251382.1:n.-413-1727_-413-1726insCT...
XM_005251326.3:c.-413-1727_-413-1726insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG XP_005251383.1:n.-413-1727_-413-1726insCT...
XM_017013948.1:c.-413-1727_-413-1726insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG XP_016869437.1:n.-413-1727_-413-1726insCT...
NM_147189.3:c.-413-1727_-413-1726insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG NP_671722.1:n.-413-1727_-413-1726insCTTTA...
NM_001377989.1:c.-413-1727_-413-1726insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG MANE Select NP_001364918.1:n.-413-1727_-413-1726insCT...
NM_001377997.1:c.-413-1727_-413-1726insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG NP_001364926.1:n.-413-1727_-413-1726insCT...
NM_001377998.1:c.-413-1727_-413-1726insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG NP_001364927.1:n.-413-1727_-413-1726insCT...
NM_147189.4:c.-413-1727_-413-1726insCTTTAATGAGCACATAGAAGAGAAATGACAGACAAGCTTGTAAAATTTGAGACTGG NP_671722.1:n.-413-1727_-413-1726insCTTTA...