Canonical Allele Identifier: CA812099492

Gene: ARL15

Linked Data

• dbSNP Id: rs1209166220
• gnomAD v3: 5-54004772-ATT-A
• gnomAD v4: 5-54004772-ATT-A
• MyVariant Identifiers: chr5:g.53300603_53300604del (hg19) ; chr5:g.54004773_54004774del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.54004775_54004776del , CM000667.2:g.54004775_54004776del	GRCh38
NC_000005.9:g.53300605_53300606del , CM000667.1:g.53300605_53300606del	GRCh37
NC_000005.8:g.53336362_53336363del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000504924.6:c.462+108428_462+108429del MANE Select	ENSP00000433427.1:n.462+108428_462+108429...
ENST00000502271.5:c.-76+108428_-76+108429del	ENSP00000473508.1:n.-76+108428_-76+108429...
ENST00000504924.5:c.462+108428_462+108429del	ENSP00000433427.1:n.462+108428_462+108429...
ENST00000507646.2:c.462+108428_462+108429del	ENSP00000432680.1:n.462+108428_462+108429...
ENST00000510591.6:n.535+108428_535+108429del
ENST00000620747.4:c.468+62388_468+62389del	ENSP00000478984.1:n.468+62388_468+62389de...
NM_019087.2:c.462+108428_462+108429del	NP_061960.1:n.462+108428_462+108429del
XM_011543498.1:c.645+108428_645+108429del	XP_011541800.1:n.645+108428_645+108429del...
XM_011543499.1:c.588+108428_588+108429del	XP_011541801.1:n.588+108428_588+108429del...
XM_011543500.1:c.519+108428_519+108429del	XP_011541802.1:n.519+108428_519+108429del...
XM_011543498.2:c.645+108428_645+108429del	XP_011541800.1:n.645+108428_645+108429del...
XM_011543499.2:c.588+108428_588+108429del	XP_011541801.1:n.588+108428_588+108429del...
XM_011543500.2:c.519+108428_519+108429del	XP_011541802.1:n.519+108428_519+108429del...
XM_017009598.1:c.468+108428_468+108429del	XP_016865087.1:n.468+108428_468+108429del...
NM_019087.3:c.462+108428_462+108429del MANE Select	NP_061960.1:n.462+108428_462+108429del