Canonical Allele Identifier: CA2725980702
Gene: PYROXD1 HGNC NCBI

Linked Data

dbSNP Id: rs2137256446

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21449502G>C , CM000674.2:g.21449502G>C GRCh38
NC_000012.11:g.21602436G>C , CM000674.1:g.21602436G>C GRCh37
NC_000012.10:g.21493703G>C NCBI36
NG_053196.1:g.16899G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000240651.14:c.286-61G>C MANE Select ENSP00000240651.9:n.286-61G>C
ENST00000240651.13:c.286-61G>C ENSP00000240651.9:n.286-61G>C
ENST00000375266.8:c.*212-61G>C ENSP00000364415.4:n.*212-61G>C
ENST00000538582.5:c.73-61G>C ENSP00000438505.1:n.73-61G>C
ENST00000543476.5:c.286-61G>C ENSP00000440192.1:n.286-61G>C
ENST00000544970.5:c.286-61G>C ENSP00000439106.1:n.286-61G>C
NM_024854.3:c.286-61G>C NP_079130.2:n.286-61G>C
XM_006719153.2:c.286-61G>C XP_006719216.1:n.286-61G>C
XR_242902.3:n.413-61G>C
NM_001350912.1:c.73-61G>C NP_001337841.1:n.73-61G>C
NM_001350913.1:c.-418-61G>C NP_001337842.1:n.-418-61G>C
NM_024854.4:c.286-61G>C NP_079130.2:n.286-61G>C
XM_006719153.3:c.286-61G>C XP_006719216.1:n.286-61G>C
XR_242902.4:n.387-61G>C
NM_024854.5:c.286-61G>C MANE Select NP_079130.2:n.286-61G>C
NM_001350913.2:c.-418-61G>C NP_001337842.1:n.-418-61G>C
NM_001350912.2:c.73-61G>C NP_001337841.1:n.73-61G>C