Canonical Allele Identifier: CA896166519

Gene: VHL

Linked Data

• MyVariant Identifiers: chr3:g.10191988G>A (hg19) ; chr3:g.10150304G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10150304G>A , CM000665.2:g.10150304G>A	GRCh38
NC_000003.11:g.10191988G>A , CM000665.1:g.10191988G>A	GRCh37
NC_000003.10:g.10166988G>A	NCBI36
NG_008212.3:g.13670G>A , LRG_322:g.13670G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000256474.3:c.*339G>A MANE Select	ENSP00000256474.3:p.=
ENST00000256474.2:c.*339G>A	ENSP00000256474.2:p.=
ENST00000345392.2:c.*339G>A	ENSP00000344757.2:p.=
NM_000551.3:c.*339G>A , LRG_322t1:c.*339G>A	NP_000542.1:p.=
NM_198156.2:c.*339G>A	NP_937799.1:p.=
NM_001354723.1:c.*535G>A	NP_001341652.1:p.=
NM_000551.4:c.*339G>A MANE Select	NP_000542.1:p.=
NM_001354723.2:c.*535G>A	NP_001341652.1:p.=
NM_198156.3:c.*339G>A	NP_937799.1:p.=