Canonical Allele Identifier: CA119210587
Gene: ARL15 HGNC NCBI

Linked Data

dbSNP Id: rs776667745
gnomAD v2: 5-53300580-C-T
gnomAD v3: 5-54004750-C-T
gnomAD v4: 5-54004750-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.54004750C>T , CM000667.2:g.54004750C>T GRCh38
NC_000005.9:g.53300580C>T , CM000667.1:g.53300580C>T GRCh37
NC_000005.8:g.53336337C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000504924.6:c.462+108452G>A MANE Select ENSP00000433427.1:n.462+108452G>A
ENST00000502271.5:c.-76+108452G>A ENSP00000473508.1:n.-76+108452G>A
ENST00000504924.5:c.462+108452G>A ENSP00000433427.1:n.462+108452G>A
ENST00000507646.2:c.462+108452G>A ENSP00000432680.1:n.462+108452G>A
ENST00000510591.6:n.535+108452G>A
ENST00000620747.4:c.468+62412G>A ENSP00000478984.1:n.468+62412G>A
NM_019087.2:c.462+108452G>A NP_061960.1:n.462+108452G>A
XM_011543498.1:c.645+108452G>A XP_011541800.1:n.645+108452G>A
XM_011543499.1:c.588+108452G>A XP_011541801.1:n.588+108452G>A
XM_011543500.1:c.519+108452G>A XP_011541802.1:n.519+108452G>A
XM_011543498.2:c.645+108452G>A XP_011541800.1:n.645+108452G>A
XM_011543499.2:c.588+108452G>A XP_011541801.1:n.588+108452G>A
XM_011543500.2:c.519+108452G>A XP_011541802.1:n.519+108452G>A
XM_017009598.1:c.468+108452G>A XP_016865087.1:n.468+108452G>A
NM_019087.3:c.462+108452G>A MANE Select NP_061960.1:n.462+108452G>A