Canonical Allele Identifier: CA2842485314

Gene: ARL15

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.54015676T>A , CM000667.2:g.54015676T>A	GRCh38
NC_000005.9:g.53311506T>A , CM000667.1:g.53311506T>A	GRCh37
NC_000005.8:g.53347263T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504924.6:c.462+97526A>T MANE Select	ENSP00000433427.1:n.462+97526A>T
ENST00000502271.5:c.-76+97526A>T	ENSP00000473508.1:n.-76+97526A>T
ENST00000504924.5:c.462+97526A>T	ENSP00000433427.1:n.462+97526A>T
ENST00000507646.2:c.462+97526A>T	ENSP00000432680.1:n.462+97526A>T
ENST00000510591.6:n.535+97526A>T
ENST00000620747.4:c.468+51486A>T	ENSP00000478984.1:n.468+51486A>T
NM_019087.2:c.462+97526A>T	NP_061960.1:n.462+97526A>T
XM_011543498.1:c.645+97526A>T	XP_011541800.1:n.645+97526A>T
XM_011543499.1:c.588+97526A>T	XP_011541801.1:n.588+97526A>T
XM_011543500.1:c.519+97526A>T	XP_011541802.1:n.519+97526A>T
XM_011543498.2:c.645+97526A>T	XP_011541800.1:n.645+97526A>T
XM_011543499.2:c.588+97526A>T	XP_011541801.1:n.588+97526A>T
XM_011543500.2:c.519+97526A>T	XP_011541802.1:n.519+97526A>T
XM_017009598.1:c.468+97526A>T	XP_016865087.1:n.468+97526A>T
NM_019087.3:c.462+97526A>T MANE Select	NP_061960.1:n.462+97526A>T