Canonical Allele Identifier: CA119210624

Gene: ARL15

Linked Data

• dbSNP Id: rs754516512
• gnomAD v3: 5-54004903-ATAT-A
• gnomAD v4: 5-54004903-ATAT-A
• MyVariant Identifiers: chr5:g.53300734_53300736del (hg19) ; chr5:g.54004904_54004906del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.54004907_54004909del , CM000667.2:g.54004907_54004909del	GRCh38
NC_000005.9:g.53300737_53300739del , CM000667.1:g.53300737_53300739del	GRCh37
NC_000005.8:g.53336494_53336496del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000504924.6:c.462+108296_462+108298del MANE Select	ENSP00000433427.1:n.462+108296_462+108298...
ENST00000502271.5:c.-76+108296_-76+108298del	ENSP00000473508.1:n.-76+108296_-76+108298...
ENST00000504924.5:c.462+108296_462+108298del	ENSP00000433427.1:n.462+108296_462+108298...
ENST00000507646.2:c.462+108296_462+108298del	ENSP00000432680.1:n.462+108296_462+108298...
ENST00000510591.6:n.535+108296_535+108298del
ENST00000620747.4:c.468+62256_468+62258del	ENSP00000478984.1:n.468+62256_468+62258de...
NM_019087.2:c.462+108296_462+108298del	NP_061960.1:n.462+108296_462+108298del
XM_011543498.1:c.645+108296_645+108298del	XP_011541800.1:n.645+108296_645+108298del...
XM_011543499.1:c.588+108296_588+108298del	XP_011541801.1:n.588+108296_588+108298del...
XM_011543500.1:c.519+108296_519+108298del	XP_011541802.1:n.519+108296_519+108298del...
XM_011543498.2:c.645+108296_645+108298del	XP_011541800.1:n.645+108296_645+108298del...
XM_011543499.2:c.588+108296_588+108298del	XP_011541801.1:n.588+108296_588+108298del...
XM_011543500.2:c.519+108296_519+108298del	XP_011541802.1:n.519+108296_519+108298del...
XM_017009598.1:c.468+108296_468+108298del	XP_016865087.1:n.468+108296_468+108298del...
NM_019087.3:c.462+108296_462+108298del MANE Select	NP_061960.1:n.462+108296_462+108298del