Canonical Allele Identifier: CA1546808653

Gene: ARL15

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53951403G= , CM000667.2:g.53951403G=	GRCh38
NC_000005.9:g.53247233G= , CM000667.1:g.53247233G=	GRCh37
NC_000005.8:g.53282990G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504924.6:c.463-64690C= MANE Select	ENSP00000433427.1:n.463-64690C=
ENST00000502271.5:c.-75-64690C=	ENSP00000473508.1:n.-75-64690C=
ENST00000504924.5:c.463-64690C=	ENSP00000433427.1:n.463-64690C=
ENST00000507646.2:c.463-64020C=	ENSP00000432680.1:n.463-64020C=
ENST00000510591.6:n.536-64690C=
ENST00000620747.4:c.469-64696C=	ENSP00000478984.1:n.469-64696C=
NM_019087.2:c.463-64690C=	NP_061960.1:n.463-64690C=
XM_011543498.1:c.646-64690C=	XP_011541800.1:n.646-64690C=
XM_011543499.1:c.589-64690C=	XP_011541801.1:n.589-64690C=
XM_011543500.1:c.520-64690C=	XP_011541802.1:n.520-64690C=
XM_011543498.2:c.646-64690C=	XP_011541800.1:n.646-64690C=
XM_011543499.2:c.589-64690C=	XP_011541801.1:n.589-64690C=
XM_011543500.2:c.520-64690C=	XP_011541802.1:n.520-64690C=
XM_017009598.1:c.469-64690C=	XP_016865087.1:n.469-64690C=
NM_019087.3:c.463-64690C= MANE Select	NP_061960.1:n.463-64690C=