Canonical Allele Identifier: CA1345063628

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10150397C= , CM000665.2:g.10150397C=	GRCh38
NC_000003.11:g.10192081C= , CM000665.1:g.10192081C=	GRCh37
NC_000003.10:g.10167081C=	NCBI36
NG_008212.3:g.13763C= , LRG_322:g.13763C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*751C=	ENSP00000512434.1:n.*751C=
ENST00000696143.1:c.1210C=	ENSP00000512435.1:n.1210C=
ENST00000696153.1:c.*432C=	ENSP00000512444.1:n.*432C=
ENST00000256474.3:c.*432C= MANE Select	ENSP00000256474.3:n.*432C=
ENST00000256474.2:c.*432C=	ENSP00000256474.2:n.*432C=
ENST00000345392.2:c.*432C=	ENSP00000344757.2:n.*432C=
NM_000551.3:c.*432C= , LRG_322t1:c.*432C=	NP_000542.1:n.*432C=
NM_198156.2:c.*432C=	NP_937799.1:n.*432C=
NM_001354723.1:c.*628C=	NP_001341652.1:n.*628C=
NM_000551.4:c.*432C= MANE Select	NP_000542.1:n.*432C=
NM_001354723.2:c.*628C=	NP_001341652.1:n.*628C=
NM_198156.3:c.*432C=	NP_937799.1:n.*432C=