Canonical Allele Identifier: CA1546832147
Gene: ARL15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.54004903_54004906delinsATAT , CM000667.2:g.54004903_54004906delinsATAT GRCh38
NC_000005.9:g.53300733_53300736delinsATAT , CM000667.1:g.53300733_53300736delinsATAT GRCh37
NC_000005.8:g.53336490_53336493delinsATAT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000504924.6:c.462+108296_462+108299delinsATAT MANE Select ENSP00000433427.1:n.462+108296_462+108299...
ENST00000502271.5:c.-76+108296_-76+108299delinsATAT ENSP00000473508.1:n.-76+108296_-76+108299...
ENST00000504924.5:c.462+108296_462+108299delinsATAT ENSP00000433427.1:n.462+108296_462+108299...
ENST00000507646.2:c.462+108296_462+108299delinsATAT ENSP00000432680.1:n.462+108296_462+108299...
ENST00000510591.6:n.535+108296_535+108299delinsATAT
ENST00000620747.4:c.468+62256_468+62259delinsATAT ENSP00000478984.1:n.468+62256_468+62259de...
NM_019087.2:c.462+108296_462+108299delinsATAT NP_061960.1:n.462+108296_462+108299delins...
XM_011543498.1:c.645+108296_645+108299delinsATAT XP_011541800.1:n.645+108296_645+108299del...
XM_011543499.1:c.588+108296_588+108299delinsATAT XP_011541801.1:n.588+108296_588+108299del...
XM_011543500.1:c.519+108296_519+108299delinsATAT XP_011541802.1:n.519+108296_519+108299del...
XM_011543498.2:c.645+108296_645+108299delinsATAT XP_011541800.1:n.645+108296_645+108299del...
XM_011543499.2:c.588+108296_588+108299delinsATAT XP_011541801.1:n.588+108296_588+108299del...
XM_011543500.2:c.519+108296_519+108299delinsATAT XP_011541802.1:n.519+108296_519+108299del...
XM_017009598.1:c.468+108296_468+108299delinsATAT XP_016865087.1:n.468+108296_468+108299del...
NM_019087.3:c.462+108296_462+108299delinsATAT MANE Select NP_061960.1:n.462+108296_462+108299delins...