Canonical Allele Identifier: CA2669049891

Gene: P3H2

Linked Data

• gnomAD v4: 3-189995557-T-TTTG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189995559_189995560insGTT , CM000665.2:g.189995559_189995560insGTT	GRCh38
NC_000003.11:g.189713348_189713349insGTT , CM000665.1:g.189713348_189713349insGTT	GRCh37
NC_000003.10:g.191196042_191196043insGTT	NCBI36
NG_031929.1:g.131880_131881insCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319332.10:c.481-116_481-115insCAA MANE Select	ENSP00000316881.5:n.481-116_481-115insCAA
ENST00000319332.9:c.481-116_481-115insCAA	ENSP00000316881.5:n.481-116_481-115insCAA
ENST00000426003.1:c.-63-116_-63-115insCAA	ENSP00000394326.1:n.-63-116_-63-115insCAA
ENST00000427335.6:c.-63-116_-63-115insCAA	ENSP00000408947.2:n.-63-116_-63-115insCAA
ENST00000444866.5:c.-63-116_-63-115insCAA	ENSP00000391374.1:n.-63-116_-63-115insCAA
NM_001134418.1:c.-63-116_-63-115insCAA	NP_001127890.1:n.-63-116_-63-115insCAA
NM_018192.3:c.481-116_481-115insCAA	NP_060662.2:n.481-116_481-115insCAA
XM_011512955.1:c.-63-116_-63-115insCAA	XP_011511257.1:n.-63-116_-63-115insCAA
NM_018192.4:c.481-116_481-115insCAA MANE Select	NP_060662.2:n.481-116_481-115insCAA
NM_001134418.2:c.-63-116_-63-115insCAA	NP_001127890.1:n.-63-116_-63-115insCAA