Canonical Allele Identifier: CA2542227933

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16824651_16824652insGA , CM000672.2:g.16824651_16824652insGA	GRCh38
NC_000010.10:g.16866650_16866651insGA , CM000672.1:g.16866650_16866651insGA	GRCh37
NC_000010.9:g.16906656_16906657insGA	NCBI36
NG_008967.1:g.310166_310167insTC , LRG_540:g.310166_310167insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.*323_*324insTC MANE Select	ENSP00000367064.4:n.*323_*324insTC
ENST00000377833.8:c.*323_*324insTC	ENSP00000367064.4:n.*323_*324insTC
NM_001081.3:c.*323_*324insTC , LRG_540t1:c.*323_*324insTC	NP_001072.2:n.*323_*324insTC
XM_011519709.1:c.*323_*324insTC	XP_011518011.1:n.*323_*324insTC
XM_011519710.1:c.*323_*324insTC	XP_011518012.1:n.*323_*324insTC
XM_011519711.1:c.*323_*324insTC	XP_011518013.1:n.*323_*324insTC
XM_011519709.2:c.*323_*324insTC	XP_011518011.1:n.*323_*324insTC
XM_011519710.2:c.*323_*324insTC	XP_011518012.1:n.*323_*324insTC
XM_011519711.3:c.*323_*324insTC	XP_011518013.1:n.*323_*324insTC
NM_001081.4:c.*323_*324insTC MANE Select	NP_001072.2:n.*323_*324insTC