Canonical Allele Identifier: CA119199619
Gene: ARL15 HGNC NCBI

Linked Data

dbSNP Id: rs566178874
gnomAD v2: 5-53247452-C-T
gnomAD v3: 5-53951622-C-T
gnomAD v4: 5-53951622-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53951622C>T , CM000667.2:g.53951622C>T GRCh38
NC_000005.9:g.53247452C>T , CM000667.1:g.53247452C>T GRCh37
NC_000005.8:g.53283209C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000504924.6:c.463-64909G>A MANE Select ENSP00000433427.1:n.463-64909G>A
ENST00000502271.5:c.-75-64909G>A ENSP00000473508.1:n.-75-64909G>A
ENST00000504924.5:c.463-64909G>A ENSP00000433427.1:n.463-64909G>A
ENST00000507646.2:c.463-64239G>A ENSP00000432680.1:n.463-64239G>A
ENST00000510591.6:n.536-64909G>A
ENST00000620747.4:c.469-64915G>A ENSP00000478984.1:n.469-64915G>A
NM_019087.2:c.463-64909G>A NP_061960.1:n.463-64909G>A
XM_011543498.1:c.646-64909G>A XP_011541800.1:n.646-64909G>A
XM_011543499.1:c.589-64909G>A XP_011541801.1:n.589-64909G>A
XM_011543500.1:c.520-64909G>A XP_011541802.1:n.520-64909G>A
XM_011543498.2:c.646-64909G>A XP_011541800.1:n.646-64909G>A
XM_011543499.2:c.589-64909G>A XP_011541801.1:n.589-64909G>A
XM_011543500.2:c.520-64909G>A XP_011541802.1:n.520-64909G>A
XM_017009598.1:c.469-64909G>A XP_016865087.1:n.469-64909G>A
NM_019087.3:c.463-64909G>A MANE Select NP_061960.1:n.463-64909G>A