Canonical Allele Identifier: CA1345064858

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10151904A= , CM000665.2:g.10151904A=	GRCh38
NC_000003.11:g.10193588A= , CM000665.1:g.10193588A=	GRCh37
NC_000003.10:g.10168588A=	NCBI36
NG_008212.3:g.15270A= , LRG_322:g.15270A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696143.1:c.2717A=	ENSP00000512435.1:n.2717A=
ENST00000696153.1:c.*1939A=	ENSP00000512444.1:n.*1939A=
ENST00000256474.3:c.*1939A= MANE Select	ENSP00000256474.3:n.*1939A=
ENST00000256474.2:c.*1939A=	ENSP00000256474.2:n.*1939A=
ENST00000345392.2:c.*1939A=	ENSP00000344757.2:n.*1939A=
NM_000551.3:c.*1939A= , LRG_322t1:c.*1939A=	NP_000542.1:n.*1939A=
NM_198156.2:c.*1939A=	NP_937799.1:n.*1939A=
NM_001354723.1:c.*2135A=	NP_001341652.1:n.*2135A=
NM_000551.4:c.*1939A= MANE Select	NP_000542.1:n.*1939A=
NM_001354723.2:c.*2135A=	NP_001341652.1:n.*2135A=
NM_198156.3:c.*1939A=	NP_937799.1:n.*1939A=