Canonical Allele Identifier: CA351754122

Gene: VHL

Linked Data

• MyVariant Identifiers: chr3:g.10188276T>C (hg19) ; chr3:g.10146592T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10146592T>C , CM000665.2:g.10146592T>C	GRCh38
NC_000003.11:g.10188276T>C , CM000665.1:g.10188276T>C	GRCh37
NC_000003.10:g.10163276T>C	NCBI36
NG_008212.3:g.9958T>C , LRG_322:g.9958T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*96T>C	ENSP00000512434.1:n.*96T>C
ENST00000696143.1:c.600-3195T>C	ENSP00000512435.1:n.600-3195T>C
ENST00000696153.1:c.419T>C	ENSP00000512444.1:p.Leu140Pro
ENST00000256474.3:c.419T>C MANE Select	ENSP00000256474.3:p.Leu140Pro
ENST00000256474.2:c.419T>C	ENSP00000256474.2:p.Leu140Pro
ENST00000345392.2:c.341-3195T>C	ENSP00000344757.2:n.341-3195T>C
ENST00000477538.1:n.555T>C
NM_000551.3:c.419T>C , LRG_322t1:c.419T>C	NP_000542.1:p.Leu140Pro
NM_198156.2:c.341-3195T>C	NP_937799.1:n.341-3195T>C
XM_011534078.1:c.*96T>C	XP_011532380.1:n.*96T>C
NM_001354723.1:c.*18-3195T>C	NP_001341652.1:n.*18-3195T>C
NM_000551.4:c.419T>C MANE Select	NP_000542.1:p.Leu140Pro
NM_001354723.2:c.*18-3195T>C	NP_001341652.1:n.*18-3195T>C
NM_198156.3:c.341-3195T>C	NP_937799.1:n.341-3195T>C