Canonical Allele Identifier: CA432423377

Gene: VHL

Linked Data

• dbSNP Id: rs1575932227
• MyVariant Identifiers: chr3:g.10191523T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10149839T>A , CM000665.2:g.10149839T>A	GRCh38
NC_000003.11:g.10191523T>A , CM000665.1:g.10191523T>A	GRCh37
NC_000003.10:g.10166523T>A	NCBI36
NG_008212.3:g.13205T>A , LRG_322:g.13205T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*193T>A	ENSP00000512434.1:n.*193T>A
ENST00000696143.1:c.652T>A	ENSP00000512435.1:n.652T>A
ENST00000696153.1:c.627T>A	ENSP00000512444.1:p.Pro209=
ENST00000256474.3:c.516T>A MANE Select	ENSP00000256474.3:p.Pro172=
ENST00000256474.2:c.516T>A	ENSP00000256474.2:p.Pro172=
ENST00000345392.2:c.393T>A	ENSP00000344757.2:p.Pro131=
ENST00000477538.1:n.652T>A
NM_000551.3:c.516T>A , LRG_322t1:c.516T>A	NP_000542.1:p.Pro172=
NM_198156.2:c.393T>A	NP_937799.1:p.Pro131=
NM_001354723.1:c.*70T>A	NP_001341652.1:n.*70T>A
NM_000551.4:c.516T>A MANE Select	NP_000542.1:p.Pro172=
NM_001354723.2:c.*70T>A	NP_001341652.1:n.*70T>A
NM_198156.3:c.393T>A	NP_937799.1:p.Pro131=