Canonical Allele Identifier: CA2021109526
Gene: PYROXD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21449604A= , CM000674.2:g.21449604A= GRCh38
NC_000012.11:g.21602538A= , CM000674.1:g.21602538A= GRCh37
NC_000012.10:g.21493805A= NCBI36
NG_053196.1:g.17001A=

Transcript Alleles

HGVS Amino-acid change
ENST00000240651.14:c.327A= MANE Select ENSP00000240651.9:p.Lys109=
ENST00000240651.13:c.327A= ENSP00000240651.9:p.Lys109=
ENST00000375266.8:c.*253A= ENSP00000364415.4:n.*253A=
ENST00000538582.5:c.114A= ENSP00000438505.1:p.Lys38=
ENST00000543476.5:c.327A= ENSP00000440192.1:p.Lys109=
ENST00000544970.5:c.327A= ENSP00000439106.1:p.Lys109=
NM_024854.3:c.327A= NP_079130.2:p.Lys109=
XM_006719153.2:c.327A= XP_006719216.1:p.Lys109=
XR_242902.3:n.454A=
NM_001350912.1:c.114A= NP_001337841.1:p.Lys38=
NM_001350913.1:c.-377A= NP_001337842.1:n.-377A=
NM_024854.4:c.327A= NP_079130.2:p.Lys109=
XM_006719153.3:c.327A= XP_006719216.1:p.Lys109=
XR_242902.4:n.428A=
NM_024854.5:c.327A= MANE Select NP_079130.2:p.Lys109=
NM_001350913.2:c.-377A= NP_001337842.1:n.-377A=
NM_001350912.2:c.114A= NP_001337841.1:p.Lys38=