Canonical Allele Identifier: CA1546832053
Gene: ARL15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.54004728_54004745delinsTGGTTACAAATTTGTAGG , CM000667.2:g.54004728_54004745delinsTGGTTACAAATTTGTAGG GRCh38
NC_000005.9:g.53300558_53300575delinsTGGTTACAAATTTGTAGG , CM000667.1:g.53300558_53300575delinsTGGTTACAAATTTGTAGG GRCh37
NC_000005.8:g.53336315_53336332delinsTGGTTACAAATTTGTAGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000504924.6:c.462+108457_462+108474delinsCCTACAAATTTGTAACCA MANE Select ENSP00000433427.1:n.462+108457_462+108474delinsCCTACAAATTTGTA...
ENST00000502271.5:c.-76+108457_-76+108474delinsCCTACAAATTTGTAACCA ENSP00000473508.1:n.-76+108457_-76+108474delinsCCTACAAATTTGTA...
ENST00000504924.5:c.462+108457_462+108474delinsCCTACAAATTTGTAACCA ENSP00000433427.1:n.462+108457_462+108474delinsCCTACAAATTTGTA...
ENST00000507646.2:c.462+108457_462+108474delinsCCTACAAATTTGTAACCA ENSP00000432680.1:n.462+108457_462+108474delinsCCTACAAATTTGTA...
ENST00000510591.6:n.535+108457_535+108474delinsCCTACAAATTTGTAACCA
ENST00000620747.4:c.468+62417_468+62434delinsCCTACAAATTTGTAACCA ENSP00000478984.1:n.468+62417_468+62434delinsCCTACAAATTTGTAAC...
NM_019087.2:c.462+108457_462+108474delinsCCTACAAATTTGTAACCA NP_061960.1:n.462+108457_462+108474delinsCCTACAAATTTGTAACCA
XM_011543498.1:c.645+108457_645+108474delinsCCTACAAATTTGTAACCA XP_011541800.1:n.645+108457_645+108474delinsCCTACAAATTTGTAACC...
XM_011543499.1:c.588+108457_588+108474delinsCCTACAAATTTGTAACCA XP_011541801.1:n.588+108457_588+108474delinsCCTACAAATTTGTAACC...
XM_011543500.1:c.519+108457_519+108474delinsCCTACAAATTTGTAACCA XP_011541802.1:n.519+108457_519+108474delinsCCTACAAATTTGTAACC...
XM_011543498.2:c.645+108457_645+108474delinsCCTACAAATTTGTAACCA XP_011541800.1:n.645+108457_645+108474delinsCCTACAAATTTGTAACC...
XM_011543499.2:c.588+108457_588+108474delinsCCTACAAATTTGTAACCA XP_011541801.1:n.588+108457_588+108474delinsCCTACAAATTTGTAACC...
XM_011543500.2:c.519+108457_519+108474delinsCCTACAAATTTGTAACCA XP_011541802.1:n.519+108457_519+108474delinsCCTACAAATTTGTAACC...
XM_017009598.1:c.468+108457_468+108474delinsCCTACAAATTTGTAACCA XP_016865087.1:n.468+108457_468+108474delinsCCTACAAATTTGTAACC...
NM_019087.3:c.462+108457_462+108474delinsCCTACAAATTTGTAACCA MANE Select NP_061960.1:n.462+108457_462+108474delinsCCTACAAATTTGTAACCA