Canonical Allele Identifier: CA812099475

Gene: ARL15

Linked Data

• dbSNP Id: rs1314693594
• gnomAD v3: 5-54004734-C-G
• gnomAD v4: 5-54004734-C-G
• MyVariant Identifiers: chr5:g.53300564C>G (hg19) ; chr5:g.54004734C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.54004734C>G , CM000667.2:g.54004734C>G	GRCh38
NC_000005.9:g.53300564C>G , CM000667.1:g.53300564C>G	GRCh37
NC_000005.8:g.53336321C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000504924.6:c.462+108468G>C MANE Select	ENSP00000433427.1:n.462+108468G>C
ENST00000502271.5:c.-76+108468G>C	ENSP00000473508.1:n.-76+108468G>C
ENST00000504924.5:c.462+108468G>C	ENSP00000433427.1:n.462+108468G>C
ENST00000507646.2:c.462+108468G>C	ENSP00000432680.1:n.462+108468G>C
ENST00000510591.6:n.535+108468G>C
ENST00000620747.4:c.468+62428G>C	ENSP00000478984.1:n.468+62428G>C
NM_019087.2:c.462+108468G>C	NP_061960.1:n.462+108468G>C
XM_011543498.1:c.645+108468G>C	XP_011541800.1:n.645+108468G>C
XM_011543499.1:c.588+108468G>C	XP_011541801.1:n.588+108468G>C
XM_011543500.1:c.519+108468G>C	XP_011541802.1:n.519+108468G>C
XM_011543498.2:c.645+108468G>C	XP_011541800.1:n.645+108468G>C
XM_011543499.2:c.588+108468G>C	XP_011541801.1:n.588+108468G>C
XM_011543500.2:c.519+108468G>C	XP_011541802.1:n.519+108468G>C
XM_017009598.1:c.468+108468G>C	XP_016865087.1:n.468+108468G>C
NM_019087.3:c.462+108468G>C MANE Select	NP_061960.1:n.462+108468G>C