Canonical Allele Identifier: CA2569119962

Gene: ARL15

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.54004868_54004869insATCG , CM000667.2:g.54004868_54004869insATCG	GRCh38
NC_000005.9:g.53300698_53300699insATCG , CM000667.1:g.53300698_53300699insATCG	GRCh37
NC_000005.8:g.53336455_53336456insATCG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504924.6:c.462+108333_462+108334insCGAT MANE Select	ENSP00000433427.1:n.462+108333_462+108334insCGAT
ENST00000502271.5:c.-76+108333_-76+108334insCGAT	ENSP00000473508.1:n.-76+108333_-76+108334insCGAT
ENST00000504924.5:c.462+108333_462+108334insCGAT	ENSP00000433427.1:n.462+108333_462+108334insCGAT
ENST00000507646.2:c.462+108333_462+108334insCGAT	ENSP00000432680.1:n.462+108333_462+108334insCGAT
ENST00000510591.6:n.535+108333_535+108334insCGAT
ENST00000620747.4:c.468+62293_468+62294insCGAT	ENSP00000478984.1:n.468+62293_468+62294insCGAT
NM_019087.2:c.462+108333_462+108334insCGAT	NP_061960.1:n.462+108333_462+108334insCGAT
XM_011543498.1:c.645+108333_645+108334insCGAT	XP_011541800.1:n.645+108333_645+108334insCGAT
XM_011543499.1:c.588+108333_588+108334insCGAT	XP_011541801.1:n.588+108333_588+108334insCGAT
XM_011543500.1:c.519+108333_519+108334insCGAT	XP_011541802.1:n.519+108333_519+108334insCGAT
XM_011543498.2:c.645+108333_645+108334insCGAT	XP_011541800.1:n.645+108333_645+108334insCGAT
XM_011543499.2:c.588+108333_588+108334insCGAT	XP_011541801.1:n.588+108333_588+108334insCGAT
XM_011543500.2:c.519+108333_519+108334insCGAT	XP_011541802.1:n.519+108333_519+108334insCGAT
XM_017009598.1:c.468+108333_468+108334insCGAT	XP_016865087.1:n.468+108333_468+108334insCGAT
NM_019087.3:c.462+108333_462+108334insCGAT MANE Select	NP_061960.1:n.462+108333_462+108334insCGAT