Canonical Allele Identifier: CA1345064603

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10141817T= , CM000665.2:g.10141817T=	GRCh38
NC_000003.11:g.10183501T= , CM000665.1:g.10183501T=	GRCh37
NC_000003.10:g.10158501T=	NCBI36
NG_008212.3:g.5183T= , LRG_322:g.5183T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.-31T=	ENSP00000512434.1:n.-31T=
ENST00000696153.1:c.-31T=	ENSP00000512444.1:n.-31T=
ENST00000256474.3:c.-31T= MANE Select	ENSP00000256474.3:n.-31T=
ENST00000256474.2:c.-31T=	ENSP00000256474.2:n.-31T=
ENST00000345392.2:c.-31T=	ENSP00000344757.2:n.-31T=
NM_000551.3:c.-31T= , LRG_322t1:c.-31T=	NP_000542.1:n.-31T=
NM_198156.2:c.-31T=	NP_937799.1:n.-31T=
XM_011534078.1:c.-31T=	XP_011532380.1:n.-31T=
NM_001354723.1:c.-31T=	NP_001341652.1:n.-31T=
NM_000551.4:c.-31T= MANE Select	NP_000542.1:n.-31T=
NM_001354723.2:c.-31T=	NP_001341652.1:n.-31T=
NM_198156.3:c.-31T=	NP_937799.1:n.-31T=