Canonical Allele Identifier: CA1893383862

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16955750_16955751delinsTA , CM000672.2:g.16955750_16955751delinsTA	GRCh38
NC_000010.10:g.16997749_16997750delinsTA , CM000672.1:g.16997749_16997750delinsTA	GRCh37
NC_000010.9:g.17037755_17037756delinsTA	NCBI36
NG_008967.1:g.179067_179068delinsTA , LRG_540:g.179067_179068delinsTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.4696-1203_4696-1202delinsTA MANE Select	ENSP00000367064.4:n.4696-1203_4696-1202de...
ENST00000377833.8:c.4696-1203_4696-1202delinsTA	ENSP00000367064.4:n.4696-1203_4696-1202de...
NM_001081.3:c.4696-1203_4696-1202delinsTA , LRG_540t1:c.4696-1203_4696-1202delinsTA	NP_001072.2:n.4696-1203_4696-1202delinsTA...
XM_011519708.1:c.4696-1203_4696-1202delinsTA	XP_011518010.1:n.4696-1203_4696-1202delin...
XM_011519709.1:c.682-1203_682-1202delinsTA	XP_011518011.1:n.682-1203_682-1202delinsT...
XM_011519710.1:c.658-1203_658-1202delinsTA	XP_011518012.1:n.658-1203_658-1202delinsT...
XM_011519711.1:c.538-1203_538-1202delinsTA	XP_011518013.1:n.538-1203_538-1202delinsT...
XM_011519708.2:c.4696-1203_4696-1202delinsTA	XP_011518010.1:n.4696-1203_4696-1202delin...
XM_011519709.2:c.682-1203_682-1202delinsTA	XP_011518011.1:n.682-1203_682-1202delinsT...
XM_011519710.2:c.658-1203_658-1202delinsTA	XP_011518012.1:n.658-1203_658-1202delinsT...
XM_011519711.3:c.538-1203_538-1202delinsTA	XP_011518013.1:n.538-1203_538-1202delinsT...
NM_001081.4:c.4696-1203_4696-1202delinsTA MANE Select	NP_001072.2:n.4696-1203_4696-1202delinsTA...