Canonical Allele Identifier: CA2669049893
Gene: P3H2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.189995559_189995560insAT , CM000665.2:g.189995559_189995560insAT GRCh38
NC_000003.11:g.189713348_189713349insAT , CM000665.1:g.189713348_189713349insAT GRCh37
NC_000003.10:g.191196042_191196043insAT NCBI36
NG_031929.1:g.131879_131880insTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000319332.10:c.481-117_481-116insTA MANE Select ENSP00000316881.5:n.481-117_481-116insTA
ENST00000319332.9:c.481-117_481-116insTA ENSP00000316881.5:n.481-117_481-116insTA
ENST00000426003.1:c.-63-117_-63-116insTA ENSP00000394326.1:n.-63-117_-63-116insTA
ENST00000427335.6:c.-63-117_-63-116insTA ENSP00000408947.2:n.-63-117_-63-116insTA
ENST00000444866.5:c.-63-117_-63-116insTA ENSP00000391374.1:n.-63-117_-63-116insTA
NM_001134418.1:c.-63-117_-63-116insTA NP_001127890.1:n.-63-117_-63-116insTA
NM_018192.3:c.481-117_481-116insTA NP_060662.2:n.481-117_481-116insTA
XM_011512955.1:c.-63-117_-63-116insTA XP_011511257.1:n.-63-117_-63-116insTA
NM_018192.4:c.481-117_481-116insTA MANE Select NP_060662.2:n.481-117_481-116insTA
NM_001134418.2:c.-63-117_-63-116insTA NP_001127890.1:n.-63-117_-63-116insTA