Canonical Allele Identifier: CA1546832136

Gene: ARL15

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.54004872_54004875delinsTTTG , CM000667.2:g.54004872_54004875delinsTTTG	GRCh38
NC_000005.9:g.53300702_53300705delinsTTTG , CM000667.1:g.53300702_53300705delinsTTTG	GRCh37
NC_000005.8:g.53336459_53336462delinsTTTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504924.6:c.462+108327_462+108330delinsCAAA MANE Select	ENSP00000433427.1:n.462+108327_462+108330delinsCAAA
ENST00000502271.5:c.-76+108327_-76+108330delinsCAAA	ENSP00000473508.1:n.-76+108327_-76+108330delinsCAAA
ENST00000504924.5:c.462+108327_462+108330delinsCAAA	ENSP00000433427.1:n.462+108327_462+108330delinsCAAA
ENST00000507646.2:c.462+108327_462+108330delinsCAAA	ENSP00000432680.1:n.462+108327_462+108330delinsCAAA
ENST00000510591.6:n.535+108327_535+108330delinsCAAA
ENST00000620747.4:c.468+62287_468+62290delinsCAAA	ENSP00000478984.1:n.468+62287_468+62290delinsCAAA
NM_019087.2:c.462+108327_462+108330delinsCAAA	NP_061960.1:n.462+108327_462+108330delinsCAAA
XM_011543498.1:c.645+108327_645+108330delinsCAAA	XP_011541800.1:n.645+108327_645+108330delinsCAAA
XM_011543499.1:c.588+108327_588+108330delinsCAAA	XP_011541801.1:n.588+108327_588+108330delinsCAAA
XM_011543500.1:c.519+108327_519+108330delinsCAAA	XP_011541802.1:n.519+108327_519+108330delinsCAAA
XM_011543498.2:c.645+108327_645+108330delinsCAAA	XP_011541800.1:n.645+108327_645+108330delinsCAAA
XM_011543499.2:c.588+108327_588+108330delinsCAAA	XP_011541801.1:n.588+108327_588+108330delinsCAAA
XM_011543500.2:c.519+108327_519+108330delinsCAAA	XP_011541802.1:n.519+108327_519+108330delinsCAAA
XM_017009598.1:c.468+108327_468+108330delinsCAAA	XP_016865087.1:n.468+108327_468+108330delinsCAAA
NM_019087.3:c.462+108327_462+108330delinsCAAA MANE Select	NP_061960.1:n.462+108327_462+108330delinsCAAA