Canonical Allele Identifier: CA1345063358

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10150165T= , CM000665.2:g.10150165T=	GRCh38
NC_000003.11:g.10191849T= , CM000665.1:g.10191849T=	GRCh37
NC_000003.10:g.10166849T=	NCBI36
NG_008212.3:g.13531T= , LRG_322:g.13531T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*519T=	ENSP00000512434.1:n.*519T=
ENST00000696143.1:c.978T=	ENSP00000512435.1:n.978T=
ENST00000696153.1:c.*200T=	ENSP00000512444.1:n.*200T=
ENST00000256474.3:c.*200T= MANE Select	ENSP00000256474.3:n.*200T=
ENST00000256474.2:c.*200T=	ENSP00000256474.2:n.*200T=
ENST00000345392.2:c.*200T=	ENSP00000344757.2:n.*200T=
NM_000551.3:c.*200T= , LRG_322t1:c.*200T=	NP_000542.1:n.*200T=
NM_198156.2:c.*200T=	NP_937799.1:n.*200T=
NM_001354723.1:c.*396T=	NP_001341652.1:n.*396T=
NM_000551.4:c.*200T= MANE Select	NP_000542.1:n.*200T=
NM_001354723.2:c.*396T=	NP_001341652.1:n.*396T=
NM_198156.3:c.*200T=	NP_937799.1:n.*200T=