Canonical Allele Identifier: CA2539339656
Gene: FAM110B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.58073877_58073878insCAAGCTTGTCTTTAATGAGC , CM000670.2:g.58073877_58073878insCAAGCTTGTCTTTAATGAGC GRCh38
NC_000008.10:g.58986436_58986437insCAAGCTTGTCTTTAATGAGC , CM000670.1:g.58986436_58986437insCAAGCTTGTCTTTAATGAGC GRCh37
NC_000008.9:g.59148990_59148991insCAAGCTTGTCTTTAATGAGC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000519262.6:c.-413-1658_-413-1657insCAAGCTTGTCTTTAATGAGC MANE Select ENSP00000509301.1:n.-413-1658_-413-1657in...
ENST00000361488.7:c.-413-1658_-413-1657insCAAGCTTGTCTTTAATGAGC ENSP00000355204.3:n.-413-1658_-413-1657in...
ENST00000518427.5:n.182-1658_182-1657insCAAGCTTGTCTTTAATGAGC
ENST00000519262.5:n.397-1658_397-1657insCAAGCTTGTCTTTAATGAGC
ENST00000520369.5:n.338-1658_338-1657insCAAGCTTGTCTTTAATGAGC
ENST00000521413.1:n.46-1658_46-1657insCAAGCTTGTCTTTAATGAGC
ENST00000522059.5:n.89-1658_89-1657insCAAGCTTGTCTTTAATGAGC
ENST00000523486.5:n.137-1658_137-1657insCAAGCTTGTCTTTAATGAGC
NM_147189.2:c.-413-1658_-413-1657insCAAGCTTGTCTTTAATGAGC NP_671722.1:n.-413-1658_-413-1657insCAAGC...
XM_005251324.1:c.-413-1658_-413-1657insCAAGCTTGTCTTTAATGAGC XP_005251381.1:n.-413-1658_-413-1657insCA...
XM_005251325.2:c.-413-1658_-413-1657insCAAGCTTGTCTTTAATGAGC XP_005251382.1:n.-413-1658_-413-1657insCA...
XM_005251326.1:c.-413-1658_-413-1657insCAAGCTTGTCTTTAATGAGC XP_005251383.1:n.-413-1658_-413-1657insCA...
XM_005251324.3:c.-413-1658_-413-1657insCAAGCTTGTCTTTAATGAGC XP_005251381.1:n.-413-1658_-413-1657insCA...
XM_005251325.3:c.-413-1658_-413-1657insCAAGCTTGTCTTTAATGAGC XP_005251382.1:n.-413-1658_-413-1657insCA...
XM_005251326.3:c.-413-1658_-413-1657insCAAGCTTGTCTTTAATGAGC XP_005251383.1:n.-413-1658_-413-1657insCA...
XM_017013948.1:c.-413-1658_-413-1657insCAAGCTTGTCTTTAATGAGC XP_016869437.1:n.-413-1658_-413-1657insCA...
NM_147189.3:c.-413-1658_-413-1657insCAAGCTTGTCTTTAATGAGC NP_671722.1:n.-413-1658_-413-1657insCAAGC...
NM_001377989.1:c.-413-1658_-413-1657insCAAGCTTGTCTTTAATGAGC MANE Select NP_001364918.1:n.-413-1658_-413-1657insCA...
NM_001377997.1:c.-413-1658_-413-1657insCAAGCTTGTCTTTAATGAGC NP_001364926.1:n.-413-1658_-413-1657insCA...
NM_001377998.1:c.-413-1658_-413-1657insCAAGCTTGTCTTTAATGAGC NP_001364927.1:n.-413-1658_-413-1657insCA...
NM_147189.4:c.-413-1658_-413-1657insCAAGCTTGTCTTTAATGAGC NP_671722.1:n.-413-1658_-413-1657insCAAGC...