Canonical Allele Identifier: CA119210601

Gene: ARL15

Linked Data

• dbSNP Id: rs978991391
• gnomAD v3: 5-54004786-T-TGC
• gnomAD v4: 5-54004786-T-TGC
• MyVariant Identifiers: chr5:g.53300616_53300617insGC (hg19) ; chr5:g.54004786_54004787insGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.54004787_54004788dup , CM000667.2:g.54004787_54004788dup	GRCh38
NC_000005.9:g.53300617_53300618dup , CM000667.1:g.53300617_53300618dup	GRCh37
NC_000005.8:g.53336374_53336375dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504924.6:c.462+108414_462+108415dup MANE Select	ENSP00000433427.1:n.462+108414_462+108415dup
ENST00000502271.5:c.-76+108414_-76+108415dup	ENSP00000473508.1:n.-76+108414_-76+108415dup
ENST00000504924.5:c.462+108414_462+108415dup	ENSP00000433427.1:n.462+108414_462+108415dup
ENST00000507646.2:c.462+108414_462+108415dup	ENSP00000432680.1:n.462+108414_462+108415dup
ENST00000510591.6:n.535+108414_535+108415dup
ENST00000620747.4:c.468+62374_468+62375dup	ENSP00000478984.1:n.468+62374_468+62375dup
NM_019087.2:c.462+108414_462+108415dup	NP_061960.1:n.462+108414_462+108415dup
XM_011543498.1:c.645+108414_645+108415dup	XP_011541800.1:n.645+108414_645+108415dup
XM_011543499.1:c.588+108414_588+108415dup	XP_011541801.1:n.588+108414_588+108415dup
XM_011543500.1:c.519+108414_519+108415dup	XP_011541802.1:n.519+108414_519+108415dup
XM_011543498.2:c.645+108414_645+108415dup	XP_011541800.1:n.645+108414_645+108415dup
XM_011543499.2:c.588+108414_588+108415dup	XP_011541801.1:n.588+108414_588+108415dup
XM_011543500.2:c.519+108414_519+108415dup	XP_011541802.1:n.519+108414_519+108415dup
XM_017009598.1:c.468+108414_468+108415dup	XP_016865087.1:n.468+108414_468+108415dup
NM_019087.3:c.462+108414_462+108415dup MANE Select	NP_061960.1:n.462+108414_462+108415dup