Canonical Allele Identifier: CA1893371476

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915847_16915848delinsAC , CM000672.2:g.16915847_16915848delinsAC	GRCh38
NC_000010.10:g.16957846_16957847delinsAC , CM000672.1:g.16957846_16957847delinsAC	GRCh37
NC_000010.9:g.16997852_16997853delinsAC	NCBI36
NG_008967.1:g.218970_218971delinsGT , LRG_540:g.218970_218971delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7183_7184delinsGT MANE Select	ENSP00000367064.4:p.Val2395=
ENST00000377833.8:c.7183_7184delinsGT	ENSP00000367064.4:p.Val2395=
NM_001081.3:c.7183_7184delinsGT , LRG_540t1:c.7183_7184delinsGT	NP_001072.2:p.Val2395=
XM_011519708.1:c.7183_7184delinsGT	XP_011518010.1:p.Val2395=
XM_011519709.1:c.3169_3170delinsGT	XP_011518011.1:p.Val1057=
XM_011519710.1:c.3145_3146delinsGT	XP_011518012.1:p.Val1049=
XM_011519711.1:c.3025_3026delinsGT	XP_011518013.1:p.Val1009=
XM_011519708.2:c.7183_7184delinsGT	XP_011518010.1:p.Val2395=
XM_011519709.2:c.3169_3170delinsGT	XP_011518011.1:p.Val1057=
XM_011519710.2:c.3145_3146delinsGT	XP_011518012.1:p.Val1049=
XM_011519711.3:c.3025_3026delinsGT	XP_011518013.1:p.Val1009=
NM_001081.4:c.7183_7184delinsGT MANE Select	NP_001072.2:p.Val2395=