Canonical Allele Identifier: CA559679607

Gene: ARL15

Linked Data

• dbSNP Id: rs1426762338
• gnomAD v2: 5-53247319-G-T
• gnomAD v4: 5-53951489-G-T
• MyVariant Identifiers: chr5:g.53247319G>T (hg19) ; chr5:g.53951489G>T (hg38)

Genomic Alleles

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

Transcript Alleles

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