Canonical Allele Identifier: CA1546808695
Gene: ARL15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53951489G= , CM000667.2:g.53951489G= GRCh38
NC_000005.9:g.53247319G= , CM000667.1:g.53247319G= GRCh37
NC_000005.8:g.53283076G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000504924.6:c.463-64776C= MANE Select ENSP00000433427.1:n.463-64776C=
ENST00000502271.5:c.-75-64776C= ENSP00000473508.1:n.-75-64776C=
ENST00000504924.5:c.463-64776C= ENSP00000433427.1:n.463-64776C=
ENST00000507646.2:c.463-64106C= ENSP00000432680.1:n.463-64106C=
ENST00000510591.6:n.536-64776C=
ENST00000620747.4:c.469-64782C= ENSP00000478984.1:n.469-64782C=
NM_019087.2:c.463-64776C= NP_061960.1:n.463-64776C=
XM_011543498.1:c.646-64776C= XP_011541800.1:n.646-64776C=
XM_011543499.1:c.589-64776C= XP_011541801.1:n.589-64776C=
XM_011543500.1:c.520-64776C= XP_011541802.1:n.520-64776C=
XM_011543498.2:c.646-64776C= XP_011541800.1:n.646-64776C=
XM_011543499.2:c.589-64776C= XP_011541801.1:n.589-64776C=
XM_011543500.2:c.520-64776C= XP_011541802.1:n.520-64776C=
XM_017009598.1:c.469-64776C= XP_016865087.1:n.469-64776C=
NM_019087.3:c.463-64776C= MANE Select NP_061960.1:n.463-64776C=