Canonical Allele Identifier: CA2021109496
Gene: PYROXD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21449592C= , CM000674.2:g.21449592C= GRCh38
NC_000012.11:g.21602526C= , CM000674.1:g.21602526C= GRCh37
NC_000012.10:g.21493793C= NCBI36
NG_053196.1:g.16989C=

Transcript Alleles

HGVS Amino-acid change
ENST00000240651.14:c.315C= MANE Select ENSP00000240651.9:p.His105=
ENST00000240651.13:c.315C= ENSP00000240651.9:p.His105=
ENST00000375266.8:c.*241C= ENSP00000364415.4:n.*241C=
ENST00000538582.5:c.102C= ENSP00000438505.1:p.His34=
ENST00000543476.5:c.315C= ENSP00000440192.1:p.His105=
ENST00000544970.5:c.315C= ENSP00000439106.1:p.His105=
NM_024854.3:c.315C= NP_079130.2:p.His105=
XM_006719153.2:c.315C= XP_006719216.1:p.His105=
XR_242902.3:n.442C=
NM_001350912.1:c.102C= NP_001337841.1:p.His34=
NM_001350913.1:c.-389C= NP_001337842.1:n.-389C=
NM_024854.4:c.315C= NP_079130.2:p.His105=
XM_006719153.3:c.315C= XP_006719216.1:p.His105=
XR_242902.4:n.416C=
NM_024854.5:c.315C= MANE Select NP_079130.2:p.His105=
NM_001350913.2:c.-389C= NP_001337842.1:n.-389C=
NM_001350912.2:c.102C= NP_001337841.1:p.His34=