Canonical Allele Identifier: CA2664400328

Gene: VHL

Linked Data

• gnomAD v4: 3-10150373-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10150373T>C , CM000665.2:g.10150373T>C	GRCh38
NC_000003.11:g.10192057T>C , CM000665.1:g.10192057T>C	GRCh37
NC_000003.10:g.10167057T>C	NCBI36
NG_008212.3:g.13739T>C , LRG_322:g.13739T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696142.1:c.*727T>C	ENSP00000512434.1:n.*727T>C
ENST00000696143.1:c.1186T>C	ENSP00000512435.1:n.1186T>C
ENST00000696153.1:c.*408T>C	ENSP00000512444.1:n.*408T>C
ENST00000256474.3:c.*408T>C MANE Select	ENSP00000256474.3:n.*408T>C
ENST00000256474.2:c.*408T>C	ENSP00000256474.2:n.*408T>C
ENST00000345392.2:c.*408T>C	ENSP00000344757.2:n.*408T>C
NM_000551.3:c.*408T>C , LRG_322t1:c.*408T>C	NP_000542.1:n.*408T>C
NM_198156.2:c.*408T>C	NP_937799.1:n.*408T>C
NM_001354723.1:c.*604T>C	NP_001341652.1:n.*604T>C
NM_000551.4:c.*408T>C MANE Select	NP_000542.1:n.*408T>C
NM_001354723.2:c.*604T>C	NP_001341652.1:n.*604T>C
NM_198156.3:c.*408T>C	NP_937799.1:n.*408T>C