Canonical Allele Identifier: CA2664402435

Gene: VHL

Linked Data

• gnomAD v4: 3-10151942-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10151942T>C , CM000665.2:g.10151942T>C	GRCh38
NC_000003.11:g.10193626T>C , CM000665.1:g.10193626T>C	GRCh37
NC_000003.10:g.10168626T>C	NCBI36
NG_008212.3:g.15308T>C , LRG_322:g.15308T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696143.1:c.2755T>C	ENSP00000512435.1:n.2755T>C
ENST00000696153.1:c.*1977T>C	ENSP00000512444.1:n.*1977T>C
ENST00000256474.3:c.*1977T>C MANE Select	ENSP00000256474.3:n.*1977T>C
ENST00000256474.2:c.*1977T>C	ENSP00000256474.2:n.*1977T>C
ENST00000345392.2:c.*1977T>C	ENSP00000344757.2:n.*1977T>C
NM_000551.3:c.*1977T>C , LRG_322t1:c.*1977T>C	NP_000542.1:n.*1977T>C
NM_198156.2:c.*1977T>C	NP_937799.1:n.*1977T>C
NM_001354723.1:c.*2173T>C	NP_001341652.1:n.*2173T>C
NM_000551.4:c.*1977T>C MANE Select	NP_000542.1:n.*1977T>C
NM_001354723.2:c.*2173T>C	NP_001341652.1:n.*2173T>C
NM_198156.3:c.*1977T>C	NP_937799.1:n.*1977T>C