Canonical Allele Identifier: CA444339920
Gene: ARL15 HGNC NCBI
MIR581 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.53247399T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53951569T>G , CM000667.2:g.53951569T>G GRCh38
NC_000005.9:g.53247399T>G , CM000667.1:g.53247399T>G GRCh37
NC_000005.8:g.53283156T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000504924.6:c.463-64856A>C (ARL15) MANE Select ENSP00000433427.1:n.463-64856A>C
ENST00000502271.5:c.-75-64856A>C (ARL15) ENSP00000473508.1:n.-75-64856A>C
ENST00000504924.5:c.463-64856A>C (ARL15) ENSP00000433427.1:n.463-64856A>C
ENST00000507646.2:c.463-64186A>C (ARL15) ENSP00000432680.1:n.463-64186A>C
ENST00000510591.6:n.536-64856A>C (ARL15)
ENST00000620747.4:c.469-64862A>C (ARL15) ENSP00000478984.1:n.469-64862A>C
NM_019087.2:c.463-64856A>C (ARL15) NP_061960.1:n.463-64856A>C
NR_030307.1:n.31A>C (MIR581)
XM_011543498.1:c.646-64856A>C (ARL15) XP_011541800.1:n.646-64856A>C
XM_011543499.1:c.589-64856A>C (ARL15) XP_011541801.1:n.589-64856A>C
XM_011543500.1:c.520-64856A>C (ARL15) XP_011541802.1:n.520-64856A>C
XM_011543498.2:c.646-64856A>C (ARL15) XP_011541800.1:n.646-64856A>C
XM_011543499.2:c.589-64856A>C (ARL15) XP_011541801.1:n.589-64856A>C
XM_011543500.2:c.520-64856A>C (ARL15) XP_011541802.1:n.520-64856A>C
XM_017009598.1:c.469-64856A>C (ARL15) XP_016865087.1:n.469-64856A>C
NM_019087.3:c.463-64856A>C (ARL15) MANE Select NP_061960.1:n.463-64856A>C