Canonical Allele Identifier: CA917476441
Gene: ARL15 HGNC NCBI

Linked Data

dbSNP Id: rs1561162665

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53951474_53951477del , CM000667.2:g.53951474_53951477del GRCh38
NC_000005.9:g.53247304_53247307del , CM000667.1:g.53247304_53247307del GRCh37
NC_000005.8:g.53283061_53283064del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000504924.6:c.463-64762_463-64759del MANE Select ENSP00000433427.1:n.463-64762_463-64759de...
ENST00000502271.5:c.-75-64762_-75-64759del ENSP00000473508.1:n.-75-64762_-75-64759de...
ENST00000504924.5:c.463-64762_463-64759del ENSP00000433427.1:n.463-64762_463-64759de...
ENST00000507646.2:c.463-64092_463-64089del ENSP00000432680.1:n.463-64092_463-64089de...
ENST00000510591.6:n.536-64762_536-64759del
ENST00000620747.4:c.469-64768_469-64765del ENSP00000478984.1:n.469-64768_469-64765de...
NM_019087.2:c.463-64762_463-64759del NP_061960.1:n.463-64762_463-64759del
XM_011543498.1:c.646-64762_646-64759del XP_011541800.1:n.646-64762_646-64759del
XM_011543499.1:c.589-64762_589-64759del XP_011541801.1:n.589-64762_589-64759del
XM_011543500.1:c.520-64762_520-64759del XP_011541802.1:n.520-64762_520-64759del
XM_011543498.2:c.646-64762_646-64759del XP_011541800.1:n.646-64762_646-64759del
XM_011543499.2:c.589-64762_589-64759del XP_011541801.1:n.589-64762_589-64759del
XM_011543500.2:c.520-64762_520-64759del XP_011541802.1:n.520-64762_520-64759del
XM_017009598.1:c.469-64762_469-64759del XP_016865087.1:n.469-64762_469-64759del
NM_019087.3:c.463-64762_463-64759del MANE Select NP_061960.1:n.463-64762_463-64759del