Canonical Allele Identifier: CA1546837194

Gene: ARL15

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.54015694A= , CM000667.2:g.54015694A=	GRCh38
NC_000005.9:g.53311524A= , CM000667.1:g.53311524A=	GRCh37
NC_000005.8:g.53347281A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000504924.6:c.462+97508T= MANE Select	ENSP00000433427.1:n.462+97508T=
ENST00000502271.5:c.-76+97508T=	ENSP00000473508.1:n.-76+97508T=
ENST00000504924.5:c.462+97508T=	ENSP00000433427.1:n.462+97508T=
ENST00000507646.2:c.462+97508T=	ENSP00000432680.1:n.462+97508T=
ENST00000510591.6:n.535+97508T=
ENST00000620747.4:c.468+51468T=	ENSP00000478984.1:n.468+51468T=
NM_019087.2:c.462+97508T=	NP_061960.1:n.462+97508T=
XM_011543498.1:c.645+97508T=	XP_011541800.1:n.645+97508T=
XM_011543499.1:c.588+97508T=	XP_011541801.1:n.588+97508T=
XM_011543500.1:c.519+97508T=	XP_011541802.1:n.519+97508T=
XM_011543498.2:c.645+97508T=	XP_011541800.1:n.645+97508T=
XM_011543499.2:c.588+97508T=	XP_011541801.1:n.588+97508T=
XM_011543500.2:c.519+97508T=	XP_011541802.1:n.519+97508T=
XM_017009598.1:c.468+97508T=	XP_016865087.1:n.468+97508T=
NM_019087.3:c.462+97508T= MANE Select	NP_061960.1:n.462+97508T=