Canonical Allele Identifier: CA1930860220

Gene: PYROXD2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.98387303A= , CM000672.2:g.98387303A=	GRCh38
NC_000010.10:g.100147060A= , CM000672.1:g.100147060A=	GRCh37
NC_000010.9:g.100137050A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370575.5:c.1452T= MANE Select	ENSP00000359607.4:p.Phe484=
ENST00000370575.4:c.1452T=	ENSP00000359607.4:p.Phe484=
ENST00000464808.1:n.308T=
ENST00000483923.5:n.2338T=
NM_032709.2:c.1452T=	NP_116098.2:p.Phe484=
XM_011540293.1:c.1554T=	XP_011538595.1:p.Phe518=
XM_011540294.1:c.1554T=	XP_011538596.1:p.Phe518=
XM_011540297.1:c.1089T=	XP_011538599.1:p.Phe363=
XM_011540298.1:c.1089T=	XP_011538600.1:p.Phe363=
XM_011540301.1:c.645T=	XP_011538603.1:p.Phe215=
XR_945839.1:n.3625T=
XR_945840.1:n.3847T=
XR_945841.1:n.3694T=
XR_945842.1:n.3472T=
XM_011540293.2:c.1554T=	XP_011538595.1:p.Phe518=
XM_011540301.2:c.645T=	XP_011538603.1:p.Phe215=
XM_017016835.1:c.1452T=	XP_016872324.1:p.Phe484=
XM_017016838.1:c.1089T=	XP_016872327.1:p.Phe363=
XM_017016839.2:c.1089T=	XP_016872328.1:p.Phe363=
XM_017016840.1:c.1089T=	XP_016872329.1:p.Phe363=
XM_017016841.1:c.1089T=	XP_016872330.1:p.Phe363=
XR_001747233.1:n.1499T=
XR_001747234.1:n.1719T=
XR_001747235.1:n.1564T=
XR_001747236.1:n.1344T=
XR_001747237.1:n.1344T=
XR_001747238.1:n.1483T=
XR_001747239.1:n.1483T=
NM_032709.3:c.1452T= MANE Select	NP_116098.2:p.Phe484=