Canonical Allele Identifier: CA5423608

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16920111C>G , CM000672.2:g.16920111C>G	GRCh38
NC_000010.10:g.16962110C>G , CM000672.1:g.16962110C>G	GRCh37
NC_000010.9:g.17002116C>G	NCBI36
NG_008967.1:g.214707G>C , LRG_540:g.214707G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.6673G>C MANE Select	NP_001072.2:p.Asp2225His
ENST00000377833.10:c.6673G>C MANE Select	ENSP00000367064.4:p.Asp2225His
NM_001081.3:c.6673G>C , LRG_540t1:c.6673G>C	NP_001072.2:p.Asp2225His
ENST00000377833.8:c.6673G>C	ENSP00000367064.4:p.Asp2225His
XM_011519708.1:c.6673G>C	XP_011518010.1:p.Asp2225His
XM_011519708.2:c.6673G>C	XP_011518010.1:p.Asp2225His
XM_011519709.1:c.2659G>C	XP_011518011.1:p.Asp887His
XM_011519709.2:c.2659G>C	XP_011518011.1:p.Asp887His
XM_011519710.1:c.2635G>C	XP_011518012.1:p.Asp879His
XM_011519710.2:c.2635G>C	XP_011518012.1:p.Asp879His
XM_011519711.1:c.2515G>C	XP_011518013.1:p.Asp839His
XM_011519711.3:c.2515G>C	XP_011518013.1:p.Asp839His