Canonical Allele Identifier: CA393660356

Gene: ARRDC4

Linked Data

• gnomAD v4: 15-97960878-G-T
• MyVariant Identifiers: chr15:g.98504108G>T (hg19) ; chr15:g.97960878G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.97960878G>T , CM000677.2:g.97960878G>T	GRCh38
NC_000015.9:g.98504108G>T , CM000677.1:g.98504108G>T	GRCh37
NC_000015.8:g.96305112G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268042.7:c.17G>T MANE Select	ENSP00000268042.6:p.Gly6Val
ENST00000268042.6:c.17G>T	ENSP00000268042.6:p.Gly6Val
NM_183376.2:c.17G>T	NP_899232.2:p.Gly6Val
NM_183376.3:c.17G>T MANE Select	NP_899232.2:p.Gly6Val