Canonical Allele Identifier: CA545548460

Gene: USF3

Linked Data

• dbSNP Id: rs1247593878
• gnomAD v2: 3-113370019-GATCA-G
• gnomAD v3: 3-113651172-GATCA-G
• gnomAD v4: 3-113651172-GATCA-G
• MyVariant Identifiers: chr3:g.113370020_113370023del (hg19) ; chr3:g.113651173_113651176del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.113651175_113651178del , CM000665.2:g.113651175_113651178del	GRCh38
NC_000003.11:g.113370022_113370025del , CM000665.1:g.113370022_113370025del	GRCh37
NC_000003.10:g.114852712_114852715del	NCBI36
NG_055006.1:g.50482_50485del

Transcript Alleles

HGVS	Amino-acid change
ENST00000316407.9:c.*3768_*3771del MANE Select	ENSP00000320794.4:n.*3768_*3771del
ENST00000316407.8:c.*3768_*3771del	ENSP00000320794.4:n.*3768_*3771del
ENST00000491165.5:c.257-1326_257-1323del	ENSP00000420752.1:n.257-1326_257-1323del
NM_001009899.3:c.*3768_*3771del	NP_001009899.3:n.*3768_*3771del
NR_111981.1:n.668-1326_668-1323del
XM_005247208.3:c.*3768_*3771del	XP_005247265.2:n.*3768_*3771del
XM_005247208.4:c.*3768_*3771del	XP_005247265.2:n.*3768_*3771del
XM_017005871.1:c.*3768_*3771del	XP_016861360.1:n.*3768_*3771del
XM_017005872.1:c.*3768_*3771del	XP_016861361.1:n.*3768_*3771del
XM_024453391.1:c.*3768_*3771del	XP_024309159.1:n.*3768_*3771del
XM_024453392.1:c.*3768_*3771del	XP_024309160.1:n.*3768_*3771del
NM_001009899.4:c.*3768_*3771del MANE Select	NP_001009899.3:n.*3768_*3771del
NR_111981.2:n.664-1326_664-1323del