Canonical Allele Identifier: CA1546832149

Gene: ARL15

Linked Data

• dbSNP Id: rs1748973260

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.54004905_54004909del , CM000667.2:g.54004905_54004909del	GRCh38
NC_000005.9:g.53300735_53300739del , CM000667.1:g.53300735_53300739del	GRCh37
NC_000005.8:g.53336492_53336496del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000504924.6:c.462+108295_462+108299del MANE Select	ENSP00000433427.1:n.462+108295_462+108299...
ENST00000502271.5:c.-76+108295_-76+108299del	ENSP00000473508.1:n.-76+108295_-76+108299...
ENST00000504924.5:c.462+108295_462+108299del	ENSP00000433427.1:n.462+108295_462+108299...
ENST00000507646.2:c.462+108295_462+108299del	ENSP00000432680.1:n.462+108295_462+108299...
ENST00000510591.6:n.535+108295_535+108299del
ENST00000620747.4:c.468+62255_468+62259del	ENSP00000478984.1:n.468+62255_468+62259de...
NM_019087.2:c.462+108295_462+108299del	NP_061960.1:n.462+108295_462+108299del
XM_011543498.1:c.645+108295_645+108299del	XP_011541800.1:n.645+108295_645+108299del...
XM_011543499.1:c.588+108295_588+108299del	XP_011541801.1:n.588+108295_588+108299del...
XM_011543500.1:c.519+108295_519+108299del	XP_011541802.1:n.519+108295_519+108299del...
XM_011543498.2:c.645+108295_645+108299del	XP_011541800.1:n.645+108295_645+108299del...
XM_011543499.2:c.588+108295_588+108299del	XP_011541801.1:n.588+108295_588+108299del...
XM_011543500.2:c.519+108295_519+108299del	XP_011541802.1:n.519+108295_519+108299del...
XM_017009598.1:c.468+108295_468+108299del	XP_016865087.1:n.468+108295_468+108299del...
NM_019087.3:c.462+108295_462+108299del MANE Select	NP_061960.1:n.462+108295_462+108299del