Canonical Allele Identifier: CA1345062134

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10149790A= , CM000665.2:g.10149790A=	GRCh38
NC_000003.11:g.10191474A= , CM000665.1:g.10191474A=	GRCh37
NC_000003.10:g.10166474A=	NCBI36
NG_008212.3:g.13156A= , LRG_322:g.13156A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*144A=	ENSP00000512434.1:n.*144A=
ENST00000696143.1:c.603A=	ENSP00000512435.1:n.603A=
ENST00000696153.1:c.578A=	ENSP00000512444.1:p.Tyr193=
ENST00000256474.3:c.467A= MANE Select	ENSP00000256474.3:p.Tyr156=
ENST00000256474.2:c.467A=	ENSP00000256474.2:p.Tyr156=
ENST00000345392.2:c.344A=	ENSP00000344757.2:p.Tyr115=
ENST00000477538.1:n.603A=
NM_000551.3:c.467A= , LRG_322t1:c.467A=	NP_000542.1:p.Tyr156=
NM_198156.2:c.344A=	NP_937799.1:p.Tyr115=
NM_001354723.1:c.*21A=	NP_001341652.1:n.*21A=
NM_000551.4:c.467A= MANE Select	NP_000542.1:p.Tyr156=
NM_001354723.2:c.*21A=	NP_001341652.1:n.*21A=
NM_198156.3:c.344A=	NP_937799.1:p.Tyr115=