Canonical Allele Identifier: CA393660579

Gene: ARRDC4

Linked Data

• dbSNP Id: rs1320418512
• gnomAD v2: 15-98504170-G-T
• gnomAD v4: 15-97960940-G-T
• MyVariant Identifiers: chr15:g.98504170G>T (hg19) ; chr15:g.97960940G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.97960940G>T , CM000677.2:g.97960940G>T	GRCh38
NC_000015.9:g.98504170G>T , CM000677.1:g.98504170G>T	GRCh37
NC_000015.8:g.96305174G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268042.7:c.79G>T MANE Select	ENSP00000268042.6:p.Glu27Ter
ENST00000268042.6:c.79G>T	ENSP00000268042.6:p.Glu27Ter
NM_183376.2:c.79G>T	NP_899232.2:p.Glu27Ter
NM_183376.3:c.79G>T MANE Select	NP_899232.2:p.Glu27Ter