Canonical Allele Identifier: CA468301645

Gene: CUBN

Linked Data

• gnomAD v4: 10-16915831-A-G
• MyVariant Identifiers: chr10:g.16957830A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915831A>G , CM000672.2:g.16915831A>G	GRCh38
NC_000010.10:g.16957830A>G , CM000672.1:g.16957830A>G	GRCh37
NC_000010.9:g.16997836A>G	NCBI36
NG_008967.1:g.218987T>C , LRG_540:g.218987T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7200T>C MANE Select	ENSP00000367064.4:p.Asn2400=
ENST00000377833.8:c.7200T>C	ENSP00000367064.4:p.Asn2400=
NM_001081.3:c.7200T>C , LRG_540t1:c.7200T>C	NP_001072.2:p.Asn2400=
XM_011519708.1:c.7200T>C	XP_011518010.1:p.Asn2400=
XM_011519709.1:c.3186T>C	XP_011518011.1:p.Asn1062=
XM_011519710.1:c.3162T>C	XP_011518012.1:p.Asn1054=
XM_011519711.1:c.3042T>C	XP_011518013.1:p.Asn1014=
XM_011519708.2:c.7200T>C	XP_011518010.1:p.Asn2400=
XM_011519709.2:c.3186T>C	XP_011518011.1:p.Asn1062=
XM_011519710.2:c.3162T>C	XP_011518012.1:p.Asn1054=
XM_011519711.3:c.3042T>C	XP_011518013.1:p.Asn1014=
NM_001081.4:c.7200T>C MANE Select	NP_001072.2:p.Asn2400=