Canonical Allele Identifier: CA393660413

Gene: ARRDC4

Linked Data

• gnomAD v4: 15-97960895-G-C
• MyVariant Identifiers: chr15:g.98504125G>C (hg19) ; chr15:g.97960895G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.97960895G>C , CM000677.2:g.97960895G>C	GRCh38
NC_000015.9:g.98504125G>C , CM000677.1:g.98504125G>C	GRCh37
NC_000015.8:g.96305129G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268042.7:c.34G>C MANE Select	ENSP00000268042.6:p.Gly12Arg
ENST00000268042.6:c.34G>C	ENSP00000268042.6:p.Gly12Arg
NM_183376.2:c.34G>C	NP_899232.2:p.Gly12Arg
NM_183376.3:c.34G>C MANE Select	NP_899232.2:p.Gly12Arg