Canonical Allele Identifier: CA648308117

Gene: USF3

Linked Data

• COSMIC: COSN24372226

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.113651083_113651084insT , CM000665.2:g.113651083_113651084insT	GRCh38
NC_000003.11:g.113369930_113369931insT , CM000665.1:g.113369930_113369931insT	GRCh37
NC_000003.10:g.114852620_114852621insT	NCBI36
NG_055006.1:g.50574_50575insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000316407.9:c.*3860_*3861insA MANE Select	ENSP00000320794.4:n.*3860_*3861insA
ENST00000316407.8:c.*3860_*3861insA	ENSP00000320794.4:n.*3860_*3861insA
ENST00000491165.5:c.257-1234_257-1233insA	ENSP00000420752.1:n.257-1234_257-1233insA...
NM_001009899.3:c.*3860_*3861insA	NP_001009899.3:n.*3860_*3861insA
NR_111981.1:n.668-1234_668-1233insA
XM_005247208.3:c.*3860_*3861insA	XP_005247265.2:n.*3860_*3861insA
XM_005247208.4:c.*3860_*3861insA	XP_005247265.2:n.*3860_*3861insA
XM_017005871.1:c.*3860_*3861insA	XP_016861360.1:n.*3860_*3861insA
XM_017005872.1:c.*3860_*3861insA	XP_016861361.1:n.*3860_*3861insA
XM_024453391.1:c.*3860_*3861insA	XP_024309159.1:n.*3860_*3861insA
XM_024453392.1:c.*3860_*3861insA	XP_024309160.1:n.*3860_*3861insA
NM_001009899.4:c.*3860_*3861insA MANE Select	NP_001009899.3:n.*3860_*3861insA
NR_111981.2:n.664-1234_664-1233insA