Canonical Allele Identifier: CA377919943

Gene: ARL3

Linked Data

• ClinVar Variation Id: 1042524
• ClinVar RCV Id: RCV001346493
• dbSNP Id: rs1177720492
• gnomAD v2: 10-104445623-G-A
• gnomAD v3: 10-102685866-G-A
• gnomAD v4: 10-102685866-G-A
• MyVariant Identifiers: chr10:g.104445623G>A (hg19) ; chr10:g.102685866G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102685866G>A , CM000672.2:g.102685866G>A	GRCh38
NC_000010.10:g.104445623G>A , CM000672.1:g.104445623G>A	GRCh37
NC_000010.9:g.104435613G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260746.6:c.451C>T MANE Select	ENSP00000260746.4:p.Arg151Ter
ENST00000260746.5:c.451C>T	ENSP00000260746.4:p.Arg151Ter
NM_004311.3:c.451C>T	NP_004302.1:p.Arg151Ter
XM_017016260.1:c.451C>T	XP_016871749.1:p.Arg151Ter
NM_004311.4:c.451C>T MANE Select	NP_004302.1:p.Arg151Ter