Canonical Allele Identifier: CA119199600
Gene: ARL15 HGNC NCBI
MIR581 HGNC NCBI

Linked Data

dbSNP Id: rs788517
gnomAD v4: 5-53951556-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53951556C>T , CM000667.2:g.53951556C>T GRCh38
NC_000005.9:g.53247386C>T , CM000667.1:g.53247386C>T GRCh37
NC_000005.8:g.53283143C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000504924.6:c.463-64843G>A (ARL15) MANE Select ENSP00000433427.1:n.463-64843G>A
ENST00000502271.5:c.-75-64843G>A (ARL15) ENSP00000473508.1:n.-75-64843G>A
ENST00000504924.5:c.463-64843G>A (ARL15) ENSP00000433427.1:n.463-64843G>A
ENST00000507646.2:c.463-64173G>A (ARL15) ENSP00000432680.1:n.463-64173G>A
ENST00000510591.6:n.536-64843G>A (ARL15)
ENST00000620747.4:c.469-64849G>A (ARL15) ENSP00000478984.1:n.469-64849G>A
NM_019087.2:c.463-64843G>A (ARL15) NP_061960.1:n.463-64843G>A
NR_030307.1:n.44G>A (MIR581)
XM_011543498.1:c.646-64843G>A (ARL15) XP_011541800.1:n.646-64843G>A
XM_011543499.1:c.589-64843G>A (ARL15) XP_011541801.1:n.589-64843G>A
XM_011543500.1:c.520-64843G>A (ARL15) XP_011541802.1:n.520-64843G>A
XM_011543498.2:c.646-64843G>A (ARL15) XP_011541800.1:n.646-64843G>A
XM_011543499.2:c.589-64843G>A (ARL15) XP_011541801.1:n.589-64843G>A
XM_011543500.2:c.520-64843G>A (ARL15) XP_011541802.1:n.520-64843G>A
XM_017009598.1:c.469-64843G>A (ARL15) XP_016865087.1:n.469-64843G>A
NM_019087.3:c.463-64843G>A (ARL15) MANE Select NP_061960.1:n.463-64843G>A