Canonical Allele Identifier: CA376120540

Gene: CUBN

Linked Data

• ClinVar Variation Id: 522329
• ClinVar RCV Id: RCV000625409
• dbSNP Id: rs1183879233
• gnomAD v2: 10-16873308-T-C
• gnomAD v3: 10-16831309-T-C
• gnomAD v4: 10-16831309-T-C
• MyVariant Identifiers: chr10:g.16873308T>C (hg19) ; chr10:g.16831309T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16831309T>C , CM000672.2:g.16831309T>C	GRCh38
NC_000010.10:g.16873308T>C , CM000672.1:g.16873308T>C	GRCh37
NC_000010.9:g.16913314T>C	NCBI36
NG_008967.1:g.303509A>G , LRG_540:g.303509A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.10471A>G MANE Select	ENSP00000367064.4:p.Ser3491Gly
ENST00000377833.8:c.10471A>G	ENSP00000367064.4:p.Ser3491Gly
NM_001081.3:c.10471A>G , LRG_540t1:c.10471A>G	NP_001072.2:p.Ser3491Gly
XM_011519709.1:c.6457A>G	XP_011518011.1:p.Ser2153Gly
XM_011519710.1:c.6433A>G	XP_011518012.1:p.Ser2145Gly
XM_011519711.1:c.6313A>G	XP_011518013.1:p.Ser2105Gly
XM_011519709.2:c.6457A>G	XP_011518011.1:p.Ser2153Gly
XM_011519710.2:c.6433A>G	XP_011518012.1:p.Ser2145Gly
XM_011519711.3:c.6313A>G	XP_011518013.1:p.Ser2105Gly
NM_001081.4:c.10471A>G MANE Select	NP_001072.2:p.Ser3491Gly