Canonical Allele Identifier: CA432421824

Gene: VHL

Linked Data

• dbSNP Id: rs1696262920
• MyVariant Identifiers: chr3:g.10188238G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10146554G>T , CM000665.2:g.10146554G>T	GRCh38
NC_000003.11:g.10188238G>T , CM000665.1:g.10188238G>T	GRCh37
NC_000003.10:g.10163238G>T	NCBI36
NG_008212.3:g.9920G>T , LRG_322:g.9920G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696142.1:c.*58G>T	ENSP00000512434.1:n.*58G>T
ENST00000696143.1:c.600-3233G>T	ENSP00000512435.1:n.600-3233G>T
ENST00000696153.1:c.381G>T	ENSP00000512444.1:p.Gly127=
ENST00000256474.3:c.381G>T MANE Select	ENSP00000256474.3:p.Gly127=
ENST00000256474.2:c.381G>T	ENSP00000256474.2:p.Gly127=
ENST00000345392.2:c.341-3233G>T	ENSP00000344757.2:n.341-3233G>T
ENST00000477538.1:n.517G>T
NM_000551.3:c.381G>T , LRG_322t1:c.381G>T	NP_000542.1:p.Gly127=
NM_198156.2:c.341-3233G>T	NP_937799.1:n.341-3233G>T
XM_011534078.1:c.*58G>T	XP_011532380.1:n.*58G>T
NM_001354723.1:c.*18-3233G>T	NP_001341652.1:n.*18-3233G>T
NM_000551.4:c.381G>T MANE Select	NP_000542.1:p.Gly127=
NM_001354723.2:c.*18-3233G>T	NP_001341652.1:n.*18-3233G>T
NM_198156.3:c.341-3233G>T	NP_937799.1:n.341-3233G>T