Canonical Allele Identifier: CA1546808688
Gene: ARL15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53951475A= , CM000667.2:g.53951475A= GRCh38
NC_000005.9:g.53247305A= , CM000667.1:g.53247305A= GRCh37
NC_000005.8:g.53283062A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000504924.6:c.463-64762T= MANE Select ENSP00000433427.1:n.463-64762T=
ENST00000502271.5:c.-75-64762T= ENSP00000473508.1:n.-75-64762T=
ENST00000504924.5:c.463-64762T= ENSP00000433427.1:n.463-64762T=
ENST00000507646.2:c.463-64092T= ENSP00000432680.1:n.463-64092T=
ENST00000510591.6:n.536-64762T=
ENST00000620747.4:c.469-64768T= ENSP00000478984.1:n.469-64768T=
NM_019087.2:c.463-64762T= NP_061960.1:n.463-64762T=
XM_011543498.1:c.646-64762T= XP_011541800.1:n.646-64762T=
XM_011543499.1:c.589-64762T= XP_011541801.1:n.589-64762T=
XM_011543500.1:c.520-64762T= XP_011541802.1:n.520-64762T=
XM_011543498.2:c.646-64762T= XP_011541800.1:n.646-64762T=
XM_011543499.2:c.589-64762T= XP_011541801.1:n.589-64762T=
XM_011543500.2:c.520-64762T= XP_011541802.1:n.520-64762T=
XM_017009598.1:c.469-64762T= XP_016865087.1:n.469-64762T=
NM_019087.3:c.463-64762T= MANE Select NP_061960.1:n.463-64762T=