Canonical Allele Identifier: CA1076156967

Gene: ARL15

Linked Data

• dbSNP Id: rs4865796
• gnomAD v3: 5-53976834-G-T
• gnomAD v4: 5-53976834-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53976834G>T , CM000667.2:g.53976834G>T	GRCh38
NC_000005.9:g.53272664G>T , CM000667.1:g.53272664G>T	GRCh37
NC_000005.8:g.53308421G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000504924.6:c.463-90121C>A MANE Select	ENSP00000433427.1:n.463-90121C>A
ENST00000502271.5:c.-75-90121C>A	ENSP00000473508.1:n.-75-90121C>A
ENST00000504924.5:c.463-90121C>A	ENSP00000433427.1:n.463-90121C>A
ENST00000507646.2:c.463-89451C>A	ENSP00000432680.1:n.463-89451C>A
ENST00000510591.6:n.536-90121C>A
ENST00000620747.4:c.469-90127C>A	ENSP00000478984.1:n.469-90127C>A
NM_019087.2:c.463-90121C>A	NP_061960.1:n.463-90121C>A
XM_011543498.1:c.646-90121C>A	XP_011541800.1:n.646-90121C>A
XM_011543499.1:c.589-90121C>A	XP_011541801.1:n.589-90121C>A
XM_011543500.1:c.520-90121C>A	XP_011541802.1:n.520-90121C>A
XM_011543498.2:c.646-90121C>A	XP_011541800.1:n.646-90121C>A
XM_011543499.2:c.589-90121C>A	XP_011541801.1:n.589-90121C>A
XM_011543500.2:c.520-90121C>A	XP_011541802.1:n.520-90121C>A
XM_017009598.1:c.469-90121C>A	XP_016865087.1:n.469-90121C>A
NM_019087.3:c.463-90121C>A MANE Select	NP_061960.1:n.463-90121C>A