Canonical Allele Identifier: CA662378358

Gene: CUBN

Linked Data

• dbSNP Id: rs2295812
• gnomAD v4: 10-17126616-T-A
• MyVariant Identifiers: chr10:g.17168615T>A (hg19) ; chr10:g.17126616T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.17126616T>A , CM000672.2:g.17126616T>A	GRCh38
NC_000010.10:g.17168615T>A , CM000672.1:g.17168615T>A	GRCh37
NC_000010.9:g.17208621T>A	NCBI36
NG_008967.1:g.8202A>T , LRG_540:g.8202A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.387+145A>T MANE Select	ENSP00000367064.4:n.387+145A>T
ENST00000377823.1:c.387+145A>T	ENSP00000367054.1:n.387+145A>T
ENST00000377833.8:c.387+145A>T	ENSP00000367064.4:n.387+145A>T
ENST00000433666.5:c.48+145A>T	ENSP00000415970.1:n.48+145A>T
NM_001081.3:c.387+145A>T , LRG_540t1:c.387+145A>T	NP_001072.2:n.387+145A>T
XM_011519708.1:c.387+145A>T	XP_011518010.1:n.387+145A>T
XM_011519708.2:c.387+145A>T	XP_011518010.1:n.387+145A>T
NM_001081.4:c.387+145A>T MANE Select	NP_001072.2:n.387+145A>T