Canonical Allele Identifier: CA1546963498

Gene: ARL15

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.54296531G>A , CM000667.2:g.54296531G>A	GRCh38
NC_000005.9:g.53592361G>A , CM000667.1:g.53592361G>A	GRCh37
NC_000005.8:g.53628118G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504924.6:c.48+13901C>T MANE Select	ENSP00000433427.1:n.48+13901C>T
ENST00000502271.5:c.-345+11357C>T	ENSP00000473508.1:n.-345+11357C>T
ENST00000504924.5:c.48+13901C>T	ENSP00000433427.1:n.48+13901C>T
ENST00000505383.1:n.142+13901C>T
ENST00000505630.5:n.145+13901C>T
ENST00000507646.2:c.48+13901C>T	ENSP00000432680.1:n.48+13901C>T
ENST00000510591.6:n.121+13764C>T
ENST00000620747.4:c.48+13901C>T	ENSP00000478984.1:n.48+13901C>T
NM_019087.2:c.48+13901C>T	NP_061960.1:n.48+13901C>T
XM_011543498.1:c.174+11357C>T	XP_011541800.1:n.174+11357C>T
XM_011543499.1:c.174+11357C>T	XP_011541801.1:n.174+11357C>T
XM_011543500.1:c.48+13901C>T	XP_011541802.1:n.48+13901C>T
XM_011543498.2:c.174+11357C>T	XP_011541800.1:n.174+11357C>T
XM_011543499.2:c.174+11357C>T	XP_011541801.1:n.174+11357C>T
XM_011543500.2:c.48+13901C>T	XP_011541802.1:n.48+13901C>T
XM_017009598.1:c.-21-11173C>T	XP_016865087.1:n.-21-11173C>T
NM_019087.3:c.48+13901C>T MANE Select	NP_061960.1:n.48+13901C>T