Canonical Allele Identifier: CA559674463

Gene: ARL15

Linked Data

• gnomAD v2: 5-53300620-T-TGC
• MyVariant Identifiers: chr5:g.53300620_53300621insGC (hg19) ; chr5:g.54004790_54004791insGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.54004791_54004792insCG , CM000667.2:g.54004791_54004792insCG	GRCh38
NC_000005.9:g.53300621_53300622insCG , CM000667.1:g.53300621_53300622insCG	GRCh37
NC_000005.8:g.53336378_53336379insCG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000504924.6:c.462+108411_462+108412insGC MANE Select	ENSP00000433427.1:n.462+108411_462+108412...
ENST00000502271.5:c.-76+108411_-76+108412insGC	ENSP00000473508.1:n.-76+108411_-76+108412...
ENST00000504924.5:c.462+108411_462+108412insGC	ENSP00000433427.1:n.462+108411_462+108412...
ENST00000507646.2:c.462+108411_462+108412insGC	ENSP00000432680.1:n.462+108411_462+108412...
ENST00000510591.6:n.535+108411_535+108412insGC
ENST00000620747.4:c.468+62371_468+62372insGC	ENSP00000478984.1:n.468+62371_468+62372in...
NM_019087.2:c.462+108411_462+108412insGC	NP_061960.1:n.462+108411_462+108412insGC
XM_011543498.1:c.645+108411_645+108412insGC	XP_011541800.1:n.645+108411_645+108412ins...
XM_011543499.1:c.588+108411_588+108412insGC	XP_011541801.1:n.588+108411_588+108412ins...
XM_011543500.1:c.519+108411_519+108412insGC	XP_011541802.1:n.519+108411_519+108412ins...
XM_011543498.2:c.645+108411_645+108412insGC	XP_011541800.1:n.645+108411_645+108412ins...
XM_011543499.2:c.588+108411_588+108412insGC	XP_011541801.1:n.588+108411_588+108412ins...
XM_011543500.2:c.519+108411_519+108412insGC	XP_011541802.1:n.519+108411_519+108412ins...
XM_017009598.1:c.468+108411_468+108412insGC	XP_016865087.1:n.468+108411_468+108412ins...
NM_019087.3:c.462+108411_462+108412insGC MANE Select	NP_061960.1:n.462+108411_462+108412insGC