Canonical Allele Identifier: CA1546832184
Gene: ARL15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.54004980_54004982delinsATG , CM000667.2:g.54004980_54004982delinsATG GRCh38
NC_000005.9:g.53300810_53300812delinsATG , CM000667.1:g.53300810_53300812delinsATG GRCh37
NC_000005.8:g.53336567_53336569delinsATG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000504924.6:c.462+108220_462+108222delinsCAT MANE Select ENSP00000433427.1:n.462+108220_462+108222...
ENST00000502271.5:c.-76+108220_-76+108222delinsCAT ENSP00000473508.1:n.-76+108220_-76+108222...
ENST00000504924.5:c.462+108220_462+108222delinsCAT ENSP00000433427.1:n.462+108220_462+108222...
ENST00000507646.2:c.462+108220_462+108222delinsCAT ENSP00000432680.1:n.462+108220_462+108222...
ENST00000510591.6:n.535+108220_535+108222delinsCAT
ENST00000620747.4:c.468+62180_468+62182delinsCAT ENSP00000478984.1:n.468+62180_468+62182de...
NM_019087.2:c.462+108220_462+108222delinsCAT NP_061960.1:n.462+108220_462+108222delins...
XM_011543498.1:c.645+108220_645+108222delinsCAT XP_011541800.1:n.645+108220_645+108222del...
XM_011543499.1:c.588+108220_588+108222delinsCAT XP_011541801.1:n.588+108220_588+108222del...
XM_011543500.1:c.519+108220_519+108222delinsCAT XP_011541802.1:n.519+108220_519+108222del...
XM_011543498.2:c.645+108220_645+108222delinsCAT XP_011541800.1:n.645+108220_645+108222del...
XM_011543499.2:c.588+108220_588+108222delinsCAT XP_011541801.1:n.588+108220_588+108222del...
XM_011543500.2:c.519+108220_519+108222delinsCAT XP_011541802.1:n.519+108220_519+108222del...
XM_017009598.1:c.468+108220_468+108222delinsCAT XP_016865087.1:n.468+108220_468+108222del...
NM_019087.3:c.462+108220_462+108222delinsCAT MANE Select NP_061960.1:n.462+108220_462+108222delins...