Canonical Allele Identifier: CA203531531

Gene: CUBN

Linked Data

• dbSNP Id: rs867933271
• MyVariant Identifiers: chr10:g.16867002G>A (hg19) ; chr10:g.16825003G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16825003G>A , CM000672.2:g.16825003G>A	GRCh38
NC_000010.10:g.16867002G>A , CM000672.1:g.16867002G>A	GRCh37
NC_000010.9:g.16907008G>A	NCBI36
NG_008967.1:g.309815C>T , LRG_540:g.309815C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.10844C>T MANE Select	ENSP00000367064.4:p.Ser3615Phe
ENST00000377833.8:c.10844C>T	ENSP00000367064.4:p.Ser3615Phe
NM_001081.3:c.10844C>T , LRG_540t1:c.10844C>T	NP_001072.2:p.Ser3615Phe
XM_011519709.1:c.6830C>T	XP_011518011.1:p.Ser2277Phe
XM_011519710.1:c.6806C>T	XP_011518012.1:p.Ser2269Phe
XM_011519711.1:c.6686C>T	XP_011518013.1:p.Ser2229Phe
XM_011519709.2:c.6830C>T	XP_011518011.1:p.Ser2277Phe
XM_011519710.2:c.6806C>T	XP_011518012.1:p.Ser2269Phe
XM_011519711.3:c.6686C>T	XP_011518013.1:p.Ser2229Phe
NM_001081.4:c.10844C>T MANE Select	NP_001072.2:p.Ser3615Phe