Canonical Allele Identifier: CA1546832146
Gene: ARL15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.54004902_54004907delinsCATATT , CM000667.2:g.54004902_54004907delinsCATATT GRCh38
NC_000005.9:g.53300732_53300737delinsCATATT , CM000667.1:g.53300732_53300737delinsCATATT GRCh37
NC_000005.8:g.53336489_53336494delinsCATATT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000504924.6:c.462+108295_462+108300delinsAATATG MANE Select ENSP00000433427.1:n.462+108295_462+108300...
ENST00000502271.5:c.-76+108295_-76+108300delinsAATATG ENSP00000473508.1:n.-76+108295_-76+108300...
ENST00000504924.5:c.462+108295_462+108300delinsAATATG ENSP00000433427.1:n.462+108295_462+108300...
ENST00000507646.2:c.462+108295_462+108300delinsAATATG ENSP00000432680.1:n.462+108295_462+108300...
ENST00000510591.6:n.535+108295_535+108300delinsAATATG
ENST00000620747.4:c.468+62255_468+62260delinsAATATG ENSP00000478984.1:n.468+62255_468+62260de...
NM_019087.2:c.462+108295_462+108300delinsAATATG NP_061960.1:n.462+108295_462+108300delins...
XM_011543498.1:c.645+108295_645+108300delinsAATATG XP_011541800.1:n.645+108295_645+108300del...
XM_011543499.1:c.588+108295_588+108300delinsAATATG XP_011541801.1:n.588+108295_588+108300del...
XM_011543500.1:c.519+108295_519+108300delinsAATATG XP_011541802.1:n.519+108295_519+108300del...
XM_011543498.2:c.645+108295_645+108300delinsAATATG XP_011541800.1:n.645+108295_645+108300del...
XM_011543499.2:c.588+108295_588+108300delinsAATATG XP_011541801.1:n.588+108295_588+108300del...
XM_011543500.2:c.519+108295_519+108300delinsAATATG XP_011541802.1:n.519+108295_519+108300del...
XM_017009598.1:c.468+108295_468+108300delinsAATATG XP_016865087.1:n.468+108295_468+108300del...
NM_019087.3:c.462+108295_462+108300delinsAATATG MANE Select NP_061960.1:n.462+108295_462+108300delins...