Canonical Allele Identifier: CA351756637

Gene: VHL

Linked Data

• MyVariant Identifiers: chr3:g.10191618A>C (hg19) ; chr3:g.10149934A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10149934A>C , CM000665.2:g.10149934A>C	GRCh38
NC_000003.11:g.10191618A>C , CM000665.1:g.10191618A>C	GRCh37
NC_000003.10:g.10166618A>C	NCBI36
NG_008212.3:g.13300A>C , LRG_322:g.13300A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*288A>C	ENSP00000512434.1:n.*288A>C
ENST00000696143.1:c.747A>C	ENSP00000512435.1:n.747A>C
ENST00000696153.1:c.722A>C	ENSP00000512444.1:p.Glu241Ala
ENST00000256474.3:c.611A>C MANE Select	ENSP00000256474.3:p.Glu204Ala
ENST00000256474.2:c.611A>C	ENSP00000256474.2:p.Glu204Ala
ENST00000345392.2:c.488A>C	ENSP00000344757.2:p.Glu163Ala
ENST00000477538.1:n.747A>C
NM_000551.3:c.611A>C , LRG_322t1:c.611A>C	NP_000542.1:p.Glu204Ala
NM_198156.2:c.488A>C	NP_937799.1:p.Glu163Ala
NM_001354723.1:c.*165A>C	NP_001341652.1:n.*165A>C
NM_000551.4:c.611A>C MANE Select	NP_000542.1:p.Glu204Ala
NM_001354723.2:c.*165A>C	NP_001341652.1:n.*165A>C
NM_198156.3:c.488A>C	NP_937799.1:p.Glu163Ala