Canonical Allele Identifier: CA2669049868

Gene: P3H2

Linked Data

• gnomAD v4: 3-189995554-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.189995554_189995555insC , CM000665.2:g.189995554_189995555insC	GRCh38
NC_000003.11:g.189713343_189713344insC , CM000665.1:g.189713343_189713344insC	GRCh37
NC_000003.10:g.191196037_191196038insC	NCBI36
NG_031929.1:g.131883_131884insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319332.10:c.481-113_481-112insG MANE Select	ENSP00000316881.5:n.481-113_481-112insG
ENST00000319332.9:c.481-113_481-112insG	ENSP00000316881.5:n.481-113_481-112insG
ENST00000426003.1:c.-63-113_-63-112insG	ENSP00000394326.1:n.-63-113_-63-112insG
ENST00000427335.6:c.-63-113_-63-112insG	ENSP00000408947.2:n.-63-113_-63-112insG
ENST00000444866.5:c.-63-113_-63-112insG	ENSP00000391374.1:n.-63-113_-63-112insG
NM_001134418.1:c.-63-113_-63-112insG	NP_001127890.1:n.-63-113_-63-112insG
NM_018192.3:c.481-113_481-112insG	NP_060662.2:n.481-113_481-112insG
XM_011512955.1:c.-63-113_-63-112insG	XP_011511257.1:n.-63-113_-63-112insG
NM_018192.4:c.481-113_481-112insG MANE Select	NP_060662.2:n.481-113_481-112insG
NM_001134418.2:c.-63-113_-63-112insG	NP_001127890.1:n.-63-113_-63-112insG