Canonical Allele Identifier: CA1345063632

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10150398T= , CM000665.2:g.10150398T=	GRCh38
NC_000003.11:g.10192082T= , CM000665.1:g.10192082T=	GRCh37
NC_000003.10:g.10167082T=	NCBI36
NG_008212.3:g.13764T= , LRG_322:g.13764T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*752T=	ENSP00000512434.1:n.*752T=
ENST00000696143.1:c.1211T=	ENSP00000512435.1:n.1211T=
ENST00000696153.1:c.*433T=	ENSP00000512444.1:n.*433T=
ENST00000256474.3:c.*433T= MANE Select	ENSP00000256474.3:n.*433T=
ENST00000256474.2:c.*433T=	ENSP00000256474.2:n.*433T=
ENST00000345392.2:c.*433T=	ENSP00000344757.2:n.*433T=
NM_000551.3:c.*433T= , LRG_322t1:c.*433T=	NP_000542.1:n.*433T=
NM_198156.2:c.*433T=	NP_937799.1:n.*433T=
NM_001354723.1:c.*629T=	NP_001341652.1:n.*629T=
NM_000551.4:c.*433T= MANE Select	NP_000542.1:n.*433T=
NM_001354723.2:c.*629T=	NP_001341652.1:n.*629T=
NM_198156.3:c.*433T=	NP_937799.1:n.*433T=