Canonical Allele Identifier: CA2608394694

Gene: CUBN

Linked Data

• gnomAD v4: 10-16915710-C-CTGCAGAGAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915717_16915718insAAGTGCAGAG , CM000672.2:g.16915717_16915718insAAGTGCAGAG	GRCh38
NC_000010.10:g.16957716_16957717insAAGTGCAGAG , CM000672.1:g.16957716_16957717insAAGTGCAGAG	GRCh37
NC_000010.9:g.16997722_16997723insAAGTGCAGAG	NCBI36
NG_008967.1:g.219107_219108insCTTCTCTGCA , LRG_540:g.219107_219108insCTTCTCTGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7210+110_7210+111insCTTCTCTGCA MANE Select	ENSP00000367064.4:n.7210+110_7210+111insCTTCTCTGCA
ENST00000377833.8:c.7210+110_7210+111insCTTCTCTGCA	ENSP00000367064.4:n.7210+110_7210+111insCTTCTCTGCA
NM_001081.3:c.7210+110_7210+111insCTTCTCTGCA , LRG_540t1:c.7210+110_7210+111insCTTCTCTGCA	NP_001072.2:n.7210+110_7210+111insCTTCTCTGCA
XM_011519708.1:c.7210+110_7210+111insCTTCTCTGCA	XP_011518010.1:n.7210+110_7210+111insCTTCTCTGCA
XM_011519709.1:c.3196+110_3196+111insCTTCTCTGCA	XP_011518011.1:n.3196+110_3196+111insCTTCTCTGCA
XM_011519710.1:c.3172+110_3172+111insCTTCTCTGCA	XP_011518012.1:n.3172+110_3172+111insCTTCTCTGCA
XM_011519711.1:c.3052+110_3052+111insCTTCTCTGCA	XP_011518013.1:n.3052+110_3052+111insCTTCTCTGCA
XM_011519708.2:c.7210+110_7210+111insCTTCTCTGCA	XP_011518010.1:n.7210+110_7210+111insCTTCTCTGCA
XM_011519709.2:c.3196+110_3196+111insCTTCTCTGCA	XP_011518011.1:n.3196+110_3196+111insCTTCTCTGCA
XM_011519710.2:c.3172+110_3172+111insCTTCTCTGCA	XP_011518012.1:n.3172+110_3172+111insCTTCTCTGCA
XM_011519711.3:c.3052+110_3052+111insCTTCTCTGCA	XP_011518013.1:n.3052+110_3052+111insCTTCTCTGCA
NM_001081.4:c.7210+110_7210+111insCTTCTCTGCA MANE Select	NP_001072.2:n.7210+110_7210+111insCTTCTCTGCA