Canonical Allele Identifier: CA1893371473

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915835_16915836delinsTC , CM000672.2:g.16915835_16915836delinsTC	GRCh38
NC_000010.10:g.16957834_16957835delinsTC , CM000672.1:g.16957834_16957835delinsTC	GRCh37
NC_000010.9:g.16997840_16997841delinsTC	NCBI36
NG_008967.1:g.218982_218983delinsGA , LRG_540:g.218982_218983delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7195_7196delinsGA MANE Select	ENSP00000367064.4:p.Asp2399=
ENST00000377833.8:c.7195_7196delinsGA	ENSP00000367064.4:p.Asp2399=
NM_001081.3:c.7195_7196delinsGA , LRG_540t1:c.7195_7196delinsGA	NP_001072.2:p.Asp2399=
XM_011519708.1:c.7195_7196delinsGA	XP_011518010.1:p.Asp2399=
XM_011519709.1:c.3181_3182delinsGA	XP_011518011.1:p.Asp1061=
XM_011519710.1:c.3157_3158delinsGA	XP_011518012.1:p.Asp1053=
XM_011519711.1:c.3037_3038delinsGA	XP_011518013.1:p.Asp1013=
XM_011519708.2:c.7195_7196delinsGA	XP_011518010.1:p.Asp2399=
XM_011519709.2:c.3181_3182delinsGA	XP_011518011.1:p.Asp1061=
XM_011519710.2:c.3157_3158delinsGA	XP_011518012.1:p.Asp1053=
XM_011519711.3:c.3037_3038delinsGA	XP_011518013.1:p.Asp1013=
NM_001081.4:c.7195_7196delinsGA MANE Select	NP_001072.2:p.Asp2399=