Canonical Allele Identifier: CA1345061922

Gene: VHL

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10149589C= , CM000665.2:g.10149589C=	GRCh38
NC_000003.11:g.10191273C= , CM000665.1:g.10191273C=	GRCh37
NC_000003.10:g.10166273C=	NCBI36
NG_008212.3:g.12955C= , LRG_322:g.12955C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*141-198C=	ENSP00000512434.1:n.*141-198C=
ENST00000696143.1:c.600-198C=	ENSP00000512435.1:n.600-198C=
ENST00000696153.1:c.575-198C=	ENSP00000512444.1:n.575-198C=
ENST00000256474.3:c.464-198C= MANE Select	ENSP00000256474.3:n.464-198C=
ENST00000256474.2:c.464-198C=	ENSP00000256474.2:n.464-198C=
ENST00000345392.2:c.341-198C=	ENSP00000344757.2:n.341-198C=
ENST00000477538.1:n.600-198C=
NM_000551.3:c.464-198C= , LRG_322t1:c.464-198C=	NP_000542.1:n.464-198C=
NM_198156.2:c.341-198C=	NP_937799.1:n.341-198C=
NM_001354723.1:c.*18-198C=	NP_001341652.1:n.*18-198C=
NM_000551.4:c.464-198C= MANE Select	NP_000542.1:n.464-198C=
NM_001354723.2:c.*18-198C=	NP_001341652.1:n.*18-198C=
NM_198156.3:c.341-198C=	NP_937799.1:n.341-198C=