Canonical Allele Identifier: CA1546832013
Gene: ARL15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.54004654T= , CM000667.2:g.54004654T= GRCh38
NC_000005.9:g.53300484T= , CM000667.1:g.53300484T= GRCh37
NC_000005.8:g.53336241T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000504924.6:c.462+108548A= MANE Select ENSP00000433427.1:n.462+108548A=
ENST00000502271.5:c.-76+108548A= ENSP00000473508.1:n.-76+108548A=
ENST00000504924.5:c.462+108548A= ENSP00000433427.1:n.462+108548A=
ENST00000507646.2:c.462+108548A= ENSP00000432680.1:n.462+108548A=
ENST00000510591.6:n.535+108548A=
ENST00000620747.4:c.468+62508A= ENSP00000478984.1:n.468+62508A=
NM_019087.2:c.462+108548A= NP_061960.1:n.462+108548A=
XM_011543498.1:c.645+108548A= XP_011541800.1:n.645+108548A=
XM_011543499.1:c.588+108548A= XP_011541801.1:n.588+108548A=
XM_011543500.1:c.519+108548A= XP_011541802.1:n.519+108548A=
XM_011543498.2:c.645+108548A= XP_011541800.1:n.645+108548A=
XM_011543499.2:c.588+108548A= XP_011541801.1:n.588+108548A=
XM_011543500.2:c.519+108548A= XP_011541802.1:n.519+108548A=
XM_017009598.1:c.468+108548A= XP_016865087.1:n.468+108548A=
NM_019087.3:c.462+108548A= MANE Select NP_061960.1:n.462+108548A=