Canonical Allele Identifier: CA812099655

Gene: ARL15

Linked Data

• dbSNP Id: rs1236729200
• MyVariant Identifiers: chr5:g.53300840_53300842del (hg19) ; chr5:g.54005010_54005012del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.54005014_54005016del , CM000667.2:g.54005014_54005016del	GRCh38
NC_000005.9:g.53300844_53300846del , CM000667.1:g.53300844_53300846del	GRCh37
NC_000005.8:g.53336601_53336603del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504924.6:c.462+108190_462+108192del MANE Select	ENSP00000433427.1:n.462+108190_462+108192del
ENST00000502271.5:c.-76+108190_-76+108192del	ENSP00000473508.1:n.-76+108190_-76+108192del
ENST00000504924.5:c.462+108190_462+108192del	ENSP00000433427.1:n.462+108190_462+108192del
ENST00000507646.2:c.462+108190_462+108192del	ENSP00000432680.1:n.462+108190_462+108192del
ENST00000510591.6:n.535+108190_535+108192del
ENST00000620747.4:c.468+62150_468+62152del	ENSP00000478984.1:n.468+62150_468+62152del
NM_019087.2:c.462+108190_462+108192del	NP_061960.1:n.462+108190_462+108192del
XM_011543498.1:c.645+108190_645+108192del	XP_011541800.1:n.645+108190_645+108192del
XM_011543499.1:c.588+108190_588+108192del	XP_011541801.1:n.588+108190_588+108192del
XM_011543500.1:c.519+108190_519+108192del	XP_011541802.1:n.519+108190_519+108192del
XM_011543498.2:c.645+108190_645+108192del	XP_011541800.1:n.645+108190_645+108192del
XM_011543499.2:c.588+108190_588+108192del	XP_011541801.1:n.588+108190_588+108192del
XM_011543500.2:c.519+108190_519+108192del	XP_011541802.1:n.519+108190_519+108192del
XM_017009598.1:c.468+108190_468+108192del	XP_016865087.1:n.468+108190_468+108192del
NM_019087.3:c.462+108190_462+108192del MANE Select	NP_061960.1:n.462+108190_462+108192del