Canonical Allele Identifier: CA812099579
Gene: ARL15 HGNC NCBI

Linked Data

dbSNP Id: rs1435066761

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.54004860_54004864del , CM000667.2:g.54004860_54004864del GRCh38
NC_000005.9:g.53300690_53300694del , CM000667.1:g.53300690_53300694del GRCh37
NC_000005.8:g.53336447_53336451del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000504924.6:c.462+108344_462+108348del MANE Select ENSP00000433427.1:n.462+108344_462+108348...
ENST00000502271.5:c.-76+108344_-76+108348del ENSP00000473508.1:n.-76+108344_-76+108348...
ENST00000504924.5:c.462+108344_462+108348del ENSP00000433427.1:n.462+108344_462+108348...
ENST00000507646.2:c.462+108344_462+108348del ENSP00000432680.1:n.462+108344_462+108348...
ENST00000510591.6:n.535+108344_535+108348del
ENST00000620747.4:c.468+62304_468+62308del ENSP00000478984.1:n.468+62304_468+62308de...
NM_019087.2:c.462+108344_462+108348del NP_061960.1:n.462+108344_462+108348del
XM_011543498.1:c.645+108344_645+108348del XP_011541800.1:n.645+108344_645+108348del...
XM_011543499.1:c.588+108344_588+108348del XP_011541801.1:n.588+108344_588+108348del...
XM_011543500.1:c.519+108344_519+108348del XP_011541802.1:n.519+108344_519+108348del...
XM_011543498.2:c.645+108344_645+108348del XP_011541800.1:n.645+108344_645+108348del...
XM_011543499.2:c.588+108344_588+108348del XP_011541801.1:n.588+108344_588+108348del...
XM_011543500.2:c.519+108344_519+108348del XP_011541802.1:n.519+108344_519+108348del...
XM_017009598.1:c.468+108344_468+108348del XP_016865087.1:n.468+108344_468+108348del...
NM_019087.3:c.462+108344_462+108348del MANE Select NP_061960.1:n.462+108344_462+108348del