Canonical Allele Identifier: CA119199602

Gene: ARL15 MIR581

Linked Data

• dbSNP Id: rs1694089
• MyVariant Identifiers: chr5:g.53247394A>C (hg19) ; chr5:g.53951564A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53951564A>C , CM000667.2:g.53951564A>C	GRCh38
NC_000005.9:g.53247394A>C , CM000667.1:g.53247394A>C	GRCh37
NC_000005.8:g.53283151A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000504924.6:c.463-64851T>G (ARL15) MANE Select	ENSP00000433427.1:n.463-64851T>G
ENST00000502271.5:c.-75-64851T>G (ARL15)	ENSP00000473508.1:n.-75-64851T>G
ENST00000504924.5:c.463-64851T>G (ARL15)	ENSP00000433427.1:n.463-64851T>G
ENST00000507646.2:c.463-64181T>G (ARL15)	ENSP00000432680.1:n.463-64181T>G
ENST00000510591.6:n.536-64851T>G (ARL15)
ENST00000620747.4:c.469-64857T>G (ARL15)	ENSP00000478984.1:n.469-64857T>G
NM_019087.2:c.463-64851T>G (ARL15)	NP_061960.1:n.463-64851T>G
NR_030307.1:n.36T>G (MIR581)
XM_011543498.1:c.646-64851T>G (ARL15)	XP_011541800.1:n.646-64851T>G
XM_011543499.1:c.589-64851T>G (ARL15)	XP_011541801.1:n.589-64851T>G
XM_011543500.1:c.520-64851T>G (ARL15)	XP_011541802.1:n.520-64851T>G
XM_011543498.2:c.646-64851T>G (ARL15)	XP_011541800.1:n.646-64851T>G
XM_011543499.2:c.589-64851T>G (ARL15)	XP_011541801.1:n.589-64851T>G
XM_011543500.2:c.520-64851T>G (ARL15)	XP_011541802.1:n.520-64851T>G
XM_017009598.1:c.469-64851T>G (ARL15)	XP_016865087.1:n.469-64851T>G
NM_019087.3:c.463-64851T>G (ARL15) MANE Select	NP_061960.1:n.463-64851T>G