Canonical Allele Identifier: CA1893313739

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16828822_16828824delinsCAG , CM000672.2:g.16828822_16828824delinsCAG	GRCh38
NC_000010.10:g.16870821_16870823delinsCAG , CM000672.1:g.16870821_16870823delinsCAG	GRCh37
NC_000010.9:g.16910827_16910829delinsCAG	NCBI36
NG_008967.1:g.305994_305996delinsCTG , LRG_540:g.305994_305996delinsCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.10745_10747delinsCTG MANE Select	ENSP00000367064.4:p.Ser3582=
ENST00000377833.8:c.10745_10747delinsCTG	ENSP00000367064.4:p.Ser3582=
NM_001081.3:c.10745_10747delinsCTG , LRG_540t1:c.10745_10747delinsCTG	NP_001072.2:p.Ser3582=
XM_011519709.1:c.6731_6733delinsCTG	XP_011518011.1:p.Ser2244=
XM_011519710.1:c.6707_6709delinsCTG	XP_011518012.1:p.Ser2236=
XM_011519711.1:c.6587_6589delinsCTG	XP_011518013.1:p.Ser2196=
XM_011519709.2:c.6731_6733delinsCTG	XP_011518011.1:p.Ser2244=
XM_011519710.2:c.6707_6709delinsCTG	XP_011518012.1:p.Ser2236=
XM_011519711.3:c.6587_6589delinsCTG	XP_011518013.1:p.Ser2196=
NM_001081.4:c.10745_10747delinsCTG MANE Select	NP_001072.2:p.Ser3582=