Canonical Allele Identifier: CA559674445
Gene: ARL15 HGNC NCBI

Linked Data

dbSNP Id: rs1331536230
gnomAD v2: 5-53300586-T-A
gnomAD v3: 5-54004756-T-A
gnomAD v4: 5-54004756-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.54004756T>A , CM000667.2:g.54004756T>A GRCh38
NC_000005.9:g.53300586T>A , CM000667.1:g.53300586T>A GRCh37
NC_000005.8:g.53336343T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000504924.6:c.462+108446A>T MANE Select ENSP00000433427.1:n.462+108446A>T
ENST00000502271.5:c.-76+108446A>T ENSP00000473508.1:n.-76+108446A>T
ENST00000504924.5:c.462+108446A>T ENSP00000433427.1:n.462+108446A>T
ENST00000507646.2:c.462+108446A>T ENSP00000432680.1:n.462+108446A>T
ENST00000510591.6:n.535+108446A>T
ENST00000620747.4:c.468+62406A>T ENSP00000478984.1:n.468+62406A>T
NM_019087.2:c.462+108446A>T NP_061960.1:n.462+108446A>T
XM_011543498.1:c.645+108446A>T XP_011541800.1:n.645+108446A>T
XM_011543499.1:c.588+108446A>T XP_011541801.1:n.588+108446A>T
XM_011543500.1:c.519+108446A>T XP_011541802.1:n.519+108446A>T
XM_011543498.2:c.645+108446A>T XP_011541800.1:n.645+108446A>T
XM_011543499.2:c.588+108446A>T XP_011541801.1:n.588+108446A>T
XM_011543500.2:c.519+108446A>T XP_011541802.1:n.519+108446A>T
XM_017009598.1:c.468+108446A>T XP_016865087.1:n.468+108446A>T
NM_019087.3:c.462+108446A>T MANE Select NP_061960.1:n.462+108446A>T