Canonical Allele Identifier: CA351756391

Gene: VHL

Linked Data

• MyVariant Identifiers: chr3:g.10191566G>T (hg19) ; chr3:g.10149882G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10149882G>T , CM000665.2:g.10149882G>T	GRCh38
NC_000003.11:g.10191566G>T , CM000665.1:g.10191566G>T	GRCh37
NC_000003.10:g.10166566G>T	NCBI36
NG_008212.3:g.13248G>T , LRG_322:g.13248G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*236G>T	ENSP00000512434.1:n.*236G>T
ENST00000696143.1:c.695G>T	ENSP00000512435.1:n.695G>T
ENST00000696153.1:c.670G>T	ENSP00000512444.1:p.Asp224Tyr
ENST00000256474.3:c.559G>T MANE Select	ENSP00000256474.3:p.Asp187Tyr
ENST00000256474.2:c.559G>T	ENSP00000256474.2:p.Asp187Tyr
ENST00000345392.2:c.436G>T	ENSP00000344757.2:p.Asp146Tyr
ENST00000477538.1:n.695G>T
NM_000551.3:c.559G>T , LRG_322t1:c.559G>T	NP_000542.1:p.Asp187Tyr
NM_198156.2:c.436G>T	NP_937799.1:p.Asp146Tyr
NM_001354723.1:c.*113G>T	NP_001341652.1:n.*113G>T
NM_000551.4:c.559G>T MANE Select	NP_000542.1:p.Asp187Tyr
NM_001354723.2:c.*113G>T	NP_001341652.1:n.*113G>T
NM_198156.3:c.436G>T	NP_937799.1:p.Asp146Tyr