Canonical Allele Identifier: CA119210638

Gene: ARL15

Linked Data

• dbSNP Id: rs1038271918
• gnomAD v3: 5-54004986-GTTTTCTTTTTCTT-G
• gnomAD v4: 5-54004986-GTTTTCTTTTTCTT-G
• MyVariant Identifiers: chr5:g.53300817_53300829del (hg19) ; chr5:g.54004987_54004999del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.54004996_54005008del , CM000667.2:g.54004996_54005008del	GRCh38
NC_000005.9:g.53300826_53300838del , CM000667.1:g.53300826_53300838del	GRCh37
NC_000005.8:g.53336583_53336595del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000504924.6:c.462+108203_462+108215del MANE Select	ENSP00000433427.1:n.462+108203_462+108215...
ENST00000502271.5:c.-76+108203_-76+108215del	ENSP00000473508.1:n.-76+108203_-76+108215...
ENST00000504924.5:c.462+108203_462+108215del	ENSP00000433427.1:n.462+108203_462+108215...
ENST00000507646.2:c.462+108203_462+108215del	ENSP00000432680.1:n.462+108203_462+108215...
ENST00000510591.6:n.535+108203_535+108215del
ENST00000620747.4:c.468+62163_468+62175del	ENSP00000478984.1:n.468+62163_468+62175de...
NM_019087.2:c.462+108203_462+108215del	NP_061960.1:n.462+108203_462+108215del
XM_011543498.1:c.645+108203_645+108215del	XP_011541800.1:n.645+108203_645+108215del...
XM_011543499.1:c.588+108203_588+108215del	XP_011541801.1:n.588+108203_588+108215del...
XM_011543500.1:c.519+108203_519+108215del	XP_011541802.1:n.519+108203_519+108215del...
XM_011543498.2:c.645+108203_645+108215del	XP_011541800.1:n.645+108203_645+108215del...
XM_011543499.2:c.588+108203_588+108215del	XP_011541801.1:n.588+108203_588+108215del...
XM_011543500.2:c.519+108203_519+108215del	XP_011541802.1:n.519+108203_519+108215del...
XM_017009598.1:c.468+108203_468+108215del	XP_016865087.1:n.468+108203_468+108215del...
NM_019087.3:c.462+108203_462+108215del MANE Select	NP_061960.1:n.462+108203_462+108215del