Canonical Allele Identifier: CA1345063453

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10150259G= , CM000665.2:g.10150259G=	GRCh38
NC_000003.11:g.10191943G= , CM000665.1:g.10191943G=	GRCh37
NC_000003.10:g.10166943G=	NCBI36
NG_008212.3:g.13625G= , LRG_322:g.13625G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*613G=	ENSP00000512434.1:n.*613G=
ENST00000696143.1:c.1072G=	ENSP00000512435.1:n.1072G=
ENST00000696153.1:c.*294G=	ENSP00000512444.1:n.*294G=
ENST00000256474.3:c.*294G= MANE Select	ENSP00000256474.3:n.*294G=
ENST00000256474.2:c.*294G=	ENSP00000256474.2:n.*294G=
ENST00000345392.2:c.*294G=	ENSP00000344757.2:n.*294G=
NM_000551.3:c.*294G= , LRG_322t1:c.*294G=	NP_000542.1:n.*294G=
NM_198156.2:c.*294G=	NP_937799.1:n.*294G=
NM_001354723.1:c.*490G=	NP_001341652.1:n.*490G=
NM_000551.4:c.*294G= MANE Select	NP_000542.1:n.*294G=
NM_001354723.2:c.*490G=	NP_001341652.1:n.*490G=
NM_198156.3:c.*294G=	NP_937799.1:n.*294G=