Canonical Allele Identifier: CA376170086

Gene: CUBN

Linked Data

• MyVariant Identifiers: chr10:g.17171729C>G (hg19) ; chr10:g.17129730C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17129730C>G , CM000672.2:g.17129730C>G	GRCh38
NC_000010.10:g.17171729C>G , CM000672.1:g.17171729C>G	GRCh37
NC_000010.9:g.17211735C>G	NCBI36
NG_008967.1:g.5088G>C , LRG_540:g.5088G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.36G>C MANE Select	ENSP00000367064.4:p.Leu12Phe
ENST00000377823.1:c.36G>C	ENSP00000367054.1:p.Leu12Phe
ENST00000377833.8:c.36G>C	ENSP00000367064.4:p.Leu12Phe
NM_001081.3:c.36G>C , LRG_540t1:c.36G>C	NP_001072.2:p.Leu12Phe
XM_011519708.1:c.36G>C	XP_011518010.1:p.Leu12Phe
XM_011519708.2:c.36G>C	XP_011518010.1:p.Leu12Phe
NM_001081.4:c.36G>C MANE Select	NP_001072.2:p.Leu12Phe