Canonical Allele Identifier: CA212244934
Gene: ARL3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2788955
ClinVar RCV Id: RCV003674406
dbSNP Id: rs376548476

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102676908C>G , CM000672.2:g.102676908C>G GRCh38
NC_000010.10:g.104436665C>G , CM000672.1:g.104436665C>G GRCh37
NC_000010.9:g.104426655C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260746.6:c.535G>C MANE Select ENSP00000260746.4:p.Ala179Pro
ENST00000260746.5:c.535G>C ENSP00000260746.4:p.Ala179Pro
NM_004311.3:c.535G>C NP_004302.1:p.Ala179Pro
XM_017016260.1:c.535G>C XP_016871749.1:p.Ala179Pro
NM_004311.4:c.535G>C MANE Select NP_004302.1:p.Ala179Pro