Canonical Allele Identifier: CA444339907

Gene: ARL15 MIR581

Linked Data

• MyVariant Identifiers: chr5:g.53247395C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53951565C>G , CM000667.2:g.53951565C>G	GRCh38
NC_000005.9:g.53247395C>G , CM000667.1:g.53247395C>G	GRCh37
NC_000005.8:g.53283152C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000504924.6:c.463-64852G>C (ARL15) MANE Select	ENSP00000433427.1:n.463-64852G>C
ENST00000502271.5:c.-75-64852G>C (ARL15)	ENSP00000473508.1:n.-75-64852G>C
ENST00000504924.5:c.463-64852G>C (ARL15)	ENSP00000433427.1:n.463-64852G>C
ENST00000507646.2:c.463-64182G>C (ARL15)	ENSP00000432680.1:n.463-64182G>C
ENST00000510591.6:n.536-64852G>C (ARL15)
ENST00000620747.4:c.469-64858G>C (ARL15)	ENSP00000478984.1:n.469-64858G>C
NM_019087.2:c.463-64852G>C (ARL15)	NP_061960.1:n.463-64852G>C
NR_030307.1:n.35G>C (MIR581)
XM_011543498.1:c.646-64852G>C (ARL15)	XP_011541800.1:n.646-64852G>C
XM_011543499.1:c.589-64852G>C (ARL15)	XP_011541801.1:n.589-64852G>C
XM_011543500.1:c.520-64852G>C (ARL15)	XP_011541802.1:n.520-64852G>C
XM_011543498.2:c.646-64852G>C (ARL15)	XP_011541800.1:n.646-64852G>C
XM_011543499.2:c.589-64852G>C (ARL15)	XP_011541801.1:n.589-64852G>C
XM_011543500.2:c.520-64852G>C (ARL15)	XP_011541802.1:n.520-64852G>C
XM_017009598.1:c.469-64852G>C (ARL15)	XP_016865087.1:n.469-64852G>C
NM_019087.3:c.463-64852G>C (ARL15) MANE Select	NP_061960.1:n.463-64852G>C