Canonical Allele Identifier: CA1345065169

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10152345T= , CM000665.2:g.10152345T=	GRCh38
NC_000003.11:g.10194029T= , CM000665.1:g.10194029T=	GRCh37
NC_000003.10:g.10169029T=	NCBI36
NG_008212.3:g.15711T= , LRG_322:g.15711T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696153.1:c.*2380T=	ENSP00000512444.1:n.*2380T=
ENST00000256474.3:c.*2380T= MANE Select	ENSP00000256474.3:n.*2380T=
NM_000551.3:c.*2380T= , LRG_322t1:c.*2380T=	NP_000542.1:n.*2380T=
NM_198156.2:c.*2380T=	NP_937799.1:n.*2380T=
NM_001354723.1:c.*2576T=	NP_001341652.1:n.*2576T=
NM_000551.4:c.*2380T= MANE Select	NP_000542.1:n.*2380T=
NM_001354723.2:c.*2576T=	NP_001341652.1:n.*2576T=
NM_198156.3:c.*2380T=	NP_937799.1:n.*2380T=