Canonical Allele Identifier: CA2608396075

Gene: CUBN

Linked Data

• gnomAD v4: 10-16824695-A-ATTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16824697_16824698insTTTT , CM000672.2:g.16824697_16824698insTTTT	GRCh38
NC_000010.10:g.16866696_16866697insTTTT , CM000672.1:g.16866696_16866697insTTTT	GRCh37
NC_000010.9:g.16906702_16906703insTTTT	NCBI36
NG_008967.1:g.310122_310123insAAAA , LRG_540:g.310122_310123insAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.*279_*280insAAAA MANE Select	ENSP00000367064.4:n.*279_*280insAAAA
ENST00000377833.8:c.*279_*280insAAAA	ENSP00000367064.4:n.*279_*280insAAAA
NM_001081.3:c.*279_*280insAAAA , LRG_540t1:c.*279_*280insAAAA	NP_001072.2:n.*279_*280insAAAA
XM_011519709.1:c.*279_*280insAAAA	XP_011518011.1:n.*279_*280insAAAA
XM_011519710.1:c.*279_*280insAAAA	XP_011518012.1:n.*279_*280insAAAA
XM_011519711.1:c.*279_*280insAAAA	XP_011518013.1:n.*279_*280insAAAA
XM_011519709.2:c.*279_*280insAAAA	XP_011518011.1:n.*279_*280insAAAA
XM_011519710.2:c.*279_*280insAAAA	XP_011518012.1:n.*279_*280insAAAA
XM_011519711.3:c.*279_*280insAAAA	XP_011518013.1:n.*279_*280insAAAA
NM_001081.4:c.*279_*280insAAAA MANE Select	NP_001072.2:n.*279_*280insAAAA