Canonical Allele Identifier: CA376169629

Gene: CUBN

Linked Data

• MyVariant Identifiers: chr10:g.17171136C>A (hg19) ; chr10:g.17129137C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17129137C>A , CM000672.2:g.17129137C>A	GRCh38
NC_000010.10:g.17171136C>A , CM000672.1:g.17171136C>A	GRCh37
NC_000010.9:g.17211142C>A	NCBI36
NG_008967.1:g.5681G>T , LRG_540:g.5681G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.236G>T MANE Select	ENSP00000367064.4:p.Ser79Ile
ENST00000377823.1:c.236G>T	ENSP00000367054.1:p.Ser79Ile
ENST00000377833.8:c.236G>T	ENSP00000367064.4:p.Ser79Ile
NM_001081.3:c.236G>T , LRG_540t1:c.236G>T	NP_001072.2:p.Ser79Ile
XM_011519708.1:c.236G>T	XP_011518010.1:p.Ser79Ile
XM_011519708.2:c.236G>T	XP_011518010.1:p.Ser79Ile
NM_001081.4:c.236G>T MANE Select	NP_001072.2:p.Ser79Ile