Canonical Allele Identifier: CA1076144960
Gene: ARL15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.54004788_54004789del , CM000667.2:g.54004788_54004789del GRCh38
NC_000005.9:g.53300618_53300619del , CM000667.1:g.53300618_53300619del GRCh37
NC_000005.8:g.53336375_53336376del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000504924.6:c.462+108413_462+108414del MANE Select ENSP00000433427.1:n.462+108413_462+108414...
ENST00000502271.5:c.-76+108413_-76+108414del ENSP00000473508.1:n.-76+108413_-76+108414...
ENST00000504924.5:c.462+108413_462+108414del ENSP00000433427.1:n.462+108413_462+108414...
ENST00000507646.2:c.462+108413_462+108414del ENSP00000432680.1:n.462+108413_462+108414...
ENST00000510591.6:n.535+108413_535+108414del
ENST00000620747.4:c.468+62373_468+62374del ENSP00000478984.1:n.468+62373_468+62374de...
NM_019087.2:c.462+108413_462+108414del NP_061960.1:n.462+108413_462+108414del
XM_011543498.1:c.645+108413_645+108414del XP_011541800.1:n.645+108413_645+108414del...
XM_011543499.1:c.588+108413_588+108414del XP_011541801.1:n.588+108413_588+108414del...
XM_011543500.1:c.519+108413_519+108414del XP_011541802.1:n.519+108413_519+108414del...
XM_011543498.2:c.645+108413_645+108414del XP_011541800.1:n.645+108413_645+108414del...
XM_011543499.2:c.588+108413_588+108414del XP_011541801.1:n.588+108413_588+108414del...
XM_011543500.2:c.519+108413_519+108414del XP_011541802.1:n.519+108413_519+108414del...
XM_017009598.1:c.468+108413_468+108414del XP_016865087.1:n.468+108413_468+108414del...
NM_019087.3:c.462+108413_462+108414del MANE Select NP_061960.1:n.462+108413_462+108414del