Canonical Allele Identifier: CA376118616

Gene: CUBN

Linked Data

• dbSNP Id: rs1427108601
• gnomAD v2: 10-16867003-A-G
• gnomAD v3: 10-16825004-A-G
• gnomAD v4: 10-16825004-A-G
• MyVariant Identifiers: chr10:g.16867003A>G (hg19) ; chr10:g.16825004A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16825004A>G , CM000672.2:g.16825004A>G	GRCh38
NC_000010.10:g.16867003A>G , CM000672.1:g.16867003A>G	GRCh37
NC_000010.9:g.16907009A>G	NCBI36
NG_008967.1:g.309814T>C , LRG_540:g.309814T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.10843T>C MANE Select	ENSP00000367064.4:p.Ser3615Pro
ENST00000377833.8:c.10843T>C	ENSP00000367064.4:p.Ser3615Pro
NM_001081.3:c.10843T>C , LRG_540t1:c.10843T>C	NP_001072.2:p.Ser3615Pro
XM_011519709.1:c.6829T>C	XP_011518011.1:p.Ser2277Pro
XM_011519710.1:c.6805T>C	XP_011518012.1:p.Ser2269Pro
XM_011519711.1:c.6685T>C	XP_011518013.1:p.Ser2229Pro
XM_011519709.2:c.6829T>C	XP_011518011.1:p.Ser2277Pro
XM_011519710.2:c.6805T>C	XP_011518012.1:p.Ser2269Pro
XM_011519711.3:c.6685T>C	XP_011518013.1:p.Ser2229Pro
NM_001081.4:c.10843T>C MANE Select	NP_001072.2:p.Ser3615Pro