Canonical Allele Identifier: CA2708891453
Gene: ARL15 HGNC NCBI

Linked Data

dbSNP Id: rs2111742419

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.54004681_54004682del , CM000667.2:g.54004681_54004682del GRCh38
NC_000005.9:g.53300511_53300512del , CM000667.1:g.53300511_53300512del GRCh37
NC_000005.8:g.53336268_53336269del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000504924.6:c.462+108522_462+108523del MANE Select ENSP00000433427.1:n.462+108522_462+108523...
ENST00000502271.5:c.-76+108522_-76+108523del ENSP00000473508.1:n.-76+108522_-76+108523...
ENST00000504924.5:c.462+108522_462+108523del ENSP00000433427.1:n.462+108522_462+108523...
ENST00000507646.2:c.462+108522_462+108523del ENSP00000432680.1:n.462+108522_462+108523...
ENST00000510591.6:n.535+108522_535+108523del
ENST00000620747.4:c.468+62482_468+62483del ENSP00000478984.1:n.468+62482_468+62483de...
NM_019087.2:c.462+108522_462+108523del NP_061960.1:n.462+108522_462+108523del
XM_011543498.1:c.645+108522_645+108523del XP_011541800.1:n.645+108522_645+108523del...
XM_011543499.1:c.588+108522_588+108523del XP_011541801.1:n.588+108522_588+108523del...
XM_011543500.1:c.519+108522_519+108523del XP_011541802.1:n.519+108522_519+108523del...
XM_011543498.2:c.645+108522_645+108523del XP_011541800.1:n.645+108522_645+108523del...
XM_011543499.2:c.588+108522_588+108523del XP_011541801.1:n.588+108522_588+108523del...
XM_011543500.2:c.519+108522_519+108523del XP_011541802.1:n.519+108522_519+108523del...
XM_017009598.1:c.468+108522_468+108523del XP_016865087.1:n.468+108522_468+108523del...
NM_019087.3:c.462+108522_462+108523del MANE Select NP_061960.1:n.462+108522_462+108523del