Canonical Allele Identifier: CA1546832099

Gene: ARL15

Linked Data

• dbSNP Id: rs1748968223

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.54004793_54004794insCC , CM000667.2:g.54004793_54004794insCC	GRCh38
NC_000005.9:g.53300623_53300624insCC , CM000667.1:g.53300623_53300624insCC	GRCh37
NC_000005.8:g.53336380_53336381insCC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000504924.6:c.462+108408_462+108409insGG MANE Select	ENSP00000433427.1:n.462+108408_462+108409...
ENST00000502271.5:c.-76+108408_-76+108409insGG	ENSP00000473508.1:n.-76+108408_-76+108409...
ENST00000504924.5:c.462+108408_462+108409insGG	ENSP00000433427.1:n.462+108408_462+108409...
ENST00000507646.2:c.462+108408_462+108409insGG	ENSP00000432680.1:n.462+108408_462+108409...
ENST00000510591.6:n.535+108408_535+108409insGG
ENST00000620747.4:c.468+62368_468+62369insGG	ENSP00000478984.1:n.468+62368_468+62369in...
NM_019087.2:c.462+108408_462+108409insGG	NP_061960.1:n.462+108408_462+108409insGG
XM_011543498.1:c.645+108408_645+108409insGG	XP_011541800.1:n.645+108408_645+108409ins...
XM_011543499.1:c.588+108408_588+108409insGG	XP_011541801.1:n.588+108408_588+108409ins...
XM_011543500.1:c.519+108408_519+108409insGG	XP_011541802.1:n.519+108408_519+108409ins...
XM_011543498.2:c.645+108408_645+108409insGG	XP_011541800.1:n.645+108408_645+108409ins...
XM_011543499.2:c.588+108408_588+108409insGG	XP_011541801.1:n.588+108408_588+108409ins...
XM_011543500.2:c.519+108408_519+108409insGG	XP_011541802.1:n.519+108408_519+108409ins...
XM_017009598.1:c.468+108408_468+108409insGG	XP_016865087.1:n.468+108408_468+108409ins...
NM_019087.3:c.462+108408_462+108409insGG MANE Select	NP_061960.1:n.462+108408_462+108409insGG