Canonical Allele Identifier: CA2021109420

Gene: PYROXD1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21449528T= , CM000674.2:g.21449528T=	GRCh38
NC_000012.11:g.21602462T= , CM000674.1:g.21602462T=	GRCh37
NC_000012.10:g.21493729T=	NCBI36
NG_053196.1:g.16925T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000240651.14:c.286-35T= MANE Select	ENSP00000240651.9:n.286-35T=
ENST00000240651.13:c.286-35T=	ENSP00000240651.9:n.286-35T=
ENST00000375266.8:c.*212-35T=	ENSP00000364415.4:n.*212-35T=
ENST00000538582.5:c.73-35T=	ENSP00000438505.1:n.73-35T=
ENST00000543476.5:c.286-35T=	ENSP00000440192.1:n.286-35T=
ENST00000544970.5:c.286-35T=	ENSP00000439106.1:n.286-35T=
NM_024854.3:c.286-35T=	NP_079130.2:n.286-35T=
XM_006719153.2:c.286-35T=	XP_006719216.1:n.286-35T=
XR_242902.3:n.413-35T=
NM_001350912.1:c.73-35T=	NP_001337841.1:n.73-35T=
NM_001350913.1:c.-418-35T=	NP_001337842.1:n.-418-35T=
NM_024854.4:c.286-35T=	NP_079130.2:n.286-35T=
XM_006719153.3:c.286-35T=	XP_006719216.1:n.286-35T=
XR_242902.4:n.387-35T=
NM_024854.5:c.286-35T= MANE Select	NP_079130.2:n.286-35T=
NM_001350913.2:c.-418-35T=	NP_001337842.1:n.-418-35T=
NM_001350912.2:c.73-35T=	NP_001337841.1:n.73-35T=