Canonical Allele Identifier: CA1893472505

Gene: CUBN

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.236G= MANE Select	ENSP00000367064.4:p.Ser79=
ENST00000377823.1:c.236G=	ENSP00000367054.1:p.Ser79=
ENST00000377833.8:c.236G=	ENSP00000367064.4:p.Ser79=
NM_001081.3:c.236G= , LRG_540t1:c.236G=	NP_001072.2:p.Ser79=
XM_011519708.1:c.236G=	XP_011518010.1:p.Ser79=
XM_011519708.2:c.236G=	XP_011518010.1:p.Ser79=
NM_001081.4:c.236G= MANE Select	NP_001072.2:p.Ser79=