Canonical Allele Identifier: CA1345063721

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10150499G= , CM000665.2:g.10150499G=	GRCh38
NC_000003.11:g.10192183G= , CM000665.1:g.10192183G=	GRCh37
NC_000003.10:g.10167183G=	NCBI36
NG_008212.3:g.13865G= , LRG_322:g.13865G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*853G=	ENSP00000512434.1:n.*853G=
ENST00000696143.1:c.1312G=	ENSP00000512435.1:n.1312G=
ENST00000696153.1:c.*534G=	ENSP00000512444.1:n.*534G=
ENST00000256474.3:c.*534G= MANE Select	ENSP00000256474.3:n.*534G=
ENST00000256474.2:c.*534G=	ENSP00000256474.2:n.*534G=
ENST00000345392.2:c.*534G=	ENSP00000344757.2:n.*534G=
NM_000551.3:c.*534G= , LRG_322t1:c.*534G=	NP_000542.1:n.*534G=
NM_198156.2:c.*534G=	NP_937799.1:n.*534G=
NM_001354723.1:c.*730G=	NP_001341652.1:n.*730G=
NM_000551.4:c.*534G= MANE Select	NP_000542.1:n.*534G=
NM_001354723.2:c.*730G=	NP_001341652.1:n.*730G=
NM_198156.3:c.*534G=	NP_937799.1:n.*534G=