Canonical Allele Identifier: CA1546808747
Gene: ARL15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53951612_53951613delinsCT , CM000667.2:g.53951612_53951613delinsCT GRCh38
NC_000005.9:g.53247442_53247443delinsCT , CM000667.1:g.53247442_53247443delinsCT GRCh37
NC_000005.8:g.53283199_53283200delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000504924.6:c.463-64900_463-64899delinsAG MANE Select ENSP00000433427.1:n.463-64900_463-64899delinsAG
ENST00000502271.5:c.-75-64900_-75-64899delinsAG ENSP00000473508.1:n.-75-64900_-75-64899delinsAG
ENST00000504924.5:c.463-64900_463-64899delinsAG ENSP00000433427.1:n.463-64900_463-64899delinsAG
ENST00000507646.2:c.463-64230_463-64229delinsAG ENSP00000432680.1:n.463-64230_463-64229delinsAG
ENST00000510591.6:n.536-64900_536-64899delinsAG
ENST00000620747.4:c.469-64906_469-64905delinsAG ENSP00000478984.1:n.469-64906_469-64905delinsAG
NM_019087.2:c.463-64900_463-64899delinsAG NP_061960.1:n.463-64900_463-64899delinsAG
XM_011543498.1:c.646-64900_646-64899delinsAG XP_011541800.1:n.646-64900_646-64899delinsAG
XM_011543499.1:c.589-64900_589-64899delinsAG XP_011541801.1:n.589-64900_589-64899delinsAG
XM_011543500.1:c.520-64900_520-64899delinsAG XP_011541802.1:n.520-64900_520-64899delinsAG
XM_011543498.2:c.646-64900_646-64899delinsAG XP_011541800.1:n.646-64900_646-64899delinsAG
XM_011543499.2:c.589-64900_589-64899delinsAG XP_011541801.1:n.589-64900_589-64899delinsAG
XM_011543500.2:c.520-64900_520-64899delinsAG XP_011541802.1:n.520-64900_520-64899delinsAG
XM_017009598.1:c.469-64900_469-64899delinsAG XP_016865087.1:n.469-64900_469-64899delinsAG
NM_019087.3:c.463-64900_463-64899delinsAG MANE Select NP_061960.1:n.463-64900_463-64899delinsAG