Canonical Allele Identifier: CA1546832027
Gene: ARL15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.54004666G= , CM000667.2:g.54004666G= GRCh38
NC_000005.9:g.53300496G= , CM000667.1:g.53300496G= GRCh37
NC_000005.8:g.53336253G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000504924.6:c.462+108536C= MANE Select ENSP00000433427.1:n.462+108536C=
ENST00000502271.5:c.-76+108536C= ENSP00000473508.1:n.-76+108536C=
ENST00000504924.5:c.462+108536C= ENSP00000433427.1:n.462+108536C=
ENST00000507646.2:c.462+108536C= ENSP00000432680.1:n.462+108536C=
ENST00000510591.6:n.535+108536C=
ENST00000620747.4:c.468+62496C= ENSP00000478984.1:n.468+62496C=
NM_019087.2:c.462+108536C= NP_061960.1:n.462+108536C=
XM_011543498.1:c.645+108536C= XP_011541800.1:n.645+108536C=
XM_011543499.1:c.588+108536C= XP_011541801.1:n.588+108536C=
XM_011543500.1:c.519+108536C= XP_011541802.1:n.519+108536C=
XM_011543498.2:c.645+108536C= XP_011541800.1:n.645+108536C=
XM_011543499.2:c.588+108536C= XP_011541801.1:n.588+108536C=
XM_011543500.2:c.519+108536C= XP_011541802.1:n.519+108536C=
XM_017009598.1:c.468+108536C= XP_016865087.1:n.468+108536C=
NM_019087.3:c.462+108536C= MANE Select NP_061960.1:n.462+108536C=