Canonical Allele Identifier: CA2021109500
Gene: PYROXD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21449595A= , CM000674.2:g.21449595A= GRCh38
NC_000012.11:g.21602529A= , CM000674.1:g.21602529A= GRCh37
NC_000012.10:g.21493796A= NCBI36
NG_053196.1:g.16992A=

Transcript Alleles

HGVS Amino-acid change
ENST00000240651.14:c.318A= MANE Select ENSP00000240651.9:p.Val106=
ENST00000240651.13:c.318A= ENSP00000240651.9:p.Val106=
ENST00000375266.8:c.*244A= ENSP00000364415.4:n.*244A=
ENST00000538582.5:c.105A= ENSP00000438505.1:p.Val35=
ENST00000543476.5:c.318A= ENSP00000440192.1:p.Val106=
ENST00000544970.5:c.318A= ENSP00000439106.1:p.Val106=
NM_024854.3:c.318A= NP_079130.2:p.Val106=
XM_006719153.2:c.318A= XP_006719216.1:p.Val106=
XR_242902.3:n.445A=
NM_001350912.1:c.105A= NP_001337841.1:p.Val35=
NM_001350913.1:c.-386A= NP_001337842.1:n.-386A=
NM_024854.4:c.318A= NP_079130.2:p.Val106=
XM_006719153.3:c.318A= XP_006719216.1:p.Val106=
XR_242902.4:n.419A=
NM_024854.5:c.318A= MANE Select NP_079130.2:p.Val106=
NM_001350913.2:c.-386A= NP_001337842.1:n.-386A=
NM_001350912.2:c.105A= NP_001337841.1:p.Val35=