Canonical Allele Identifier: CA1345063609

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10150383C= , CM000665.2:g.10150383C=	GRCh38
NC_000003.11:g.10192067C= , CM000665.1:g.10192067C=	GRCh37
NC_000003.10:g.10167067C=	NCBI36
NG_008212.3:g.13749C= , LRG_322:g.13749C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*737C=	ENSP00000512434.1:n.*737C=
ENST00000696143.1:c.1196C=	ENSP00000512435.1:n.1196C=
ENST00000696153.1:c.*418C=	ENSP00000512444.1:n.*418C=
ENST00000256474.3:c.*418C= MANE Select	ENSP00000256474.3:n.*418C=
ENST00000256474.2:c.*418C=	ENSP00000256474.2:n.*418C=
ENST00000345392.2:c.*418C=	ENSP00000344757.2:n.*418C=
NM_000551.3:c.*418C= , LRG_322t1:c.*418C=	NP_000542.1:n.*418C=
NM_198156.2:c.*418C=	NP_937799.1:n.*418C=
NM_001354723.1:c.*614C=	NP_001341652.1:n.*614C=
NM_000551.4:c.*418C= MANE Select	NP_000542.1:n.*418C=
NM_001354723.2:c.*614C=	NP_001341652.1:n.*614C=
NM_198156.3:c.*418C=	NP_937799.1:n.*418C=