Canonical Allele Identifier: CA156576659
Gene: WIPF3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.29881908G>C , CM000669.2:g.29881908G>C GRCh38
NC_000007.13:g.29921524G>C , CM000669.1:g.29921524G>C GRCh37
NC_000007.12:g.29888049G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000242140.10:c.356-1942G>C MANE Select ENSP00000242140.6:n.356-1942G>C
ENST00000242140.9:c.356-1942G>C ENSP00000242140.6:n.356-1942G>C
ENST00000409123.5:c.356-1942G>C ENSP00000386790.1:n.356-1942G>C
ENST00000409290.1:c.356-1942G>C ENSP00000386878.1:n.356-1942G>C
NM_001080529.2:c.356-1942G>C NP_001073998.2:n.356-1942G>C
XM_011515475.1:c.848-1942G>C XP_011513777.1:n.848-1942G>C
XM_017012522.1:c.323-1942G>C XP_016868011.1:n.323-1942G>C
NM_001080529.3:c.356-1942G>C MANE Select NP_001073998.2:n.356-1942G>C
NM_001391973.1:c.356-1942G>C NP_001378902.1:n.356-1942G>C