Canonical Allele Identifier: CA2021109421
Gene: PYROXD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21449529C= , CM000674.2:g.21449529C= GRCh38
NC_000012.11:g.21602463C= , CM000674.1:g.21602463C= GRCh37
NC_000012.10:g.21493730C= NCBI36
NG_053196.1:g.16926C=

Transcript Alleles

HGVS Amino-acid change
ENST00000240651.14:c.286-34C= MANE Select ENSP00000240651.9:n.286-34C=
ENST00000240651.13:c.286-34C= ENSP00000240651.9:n.286-34C=
ENST00000375266.8:c.*212-34C= ENSP00000364415.4:n.*212-34C=
ENST00000538582.5:c.73-34C= ENSP00000438505.1:n.73-34C=
ENST00000543476.5:c.286-34C= ENSP00000440192.1:n.286-34C=
ENST00000544970.5:c.286-34C= ENSP00000439106.1:n.286-34C=
NM_024854.3:c.286-34C= NP_079130.2:n.286-34C=
XM_006719153.2:c.286-34C= XP_006719216.1:n.286-34C=
XR_242902.3:n.413-34C=
NM_001350912.1:c.73-34C= NP_001337841.1:n.73-34C=
NM_001350913.1:c.-418-34C= NP_001337842.1:n.-418-34C=
NM_024854.4:c.286-34C= NP_079130.2:n.286-34C=
XM_006719153.3:c.286-34C= XP_006719216.1:n.286-34C=
XR_242902.4:n.387-34C=
NM_024854.5:c.286-34C= MANE Select NP_079130.2:n.286-34C=
NM_001350913.2:c.-418-34C= NP_001337842.1:n.-418-34C=
NM_001350912.2:c.73-34C= NP_001337841.1:n.73-34C=