Canonical Allele Identifier: CA2473784855
Gene: MMACHC HGNC NCBI
PRDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45511022A= , CM000663.2:g.45511022A= GRCh38
NC_000001.10:g.45976694A= , CM000663.1:g.45976694A= GRCh37
NC_000001.9:g.45749281A= NCBI36
NG_013378.1:g.15839A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000401061.9:c.*1807A= (MMACHC) MANE Select ENSP00000383840.4:n.*1807A=
ENST00000424390.2:c.*307T= (PRDX1) ENSP00000389047.2:n.*307T=
ENST00000447184.6:c.*307T= (PRDX1) ENSP00000407034.2:n.*307T=
ENST00000676549.1:c.*307T= (PRDX1) ENSP00000503140.1:n.*307T=
ENST00000401061.8:c.*1807A= (MMACHC) ENSP00000383840.4:n.*1807A=
ENST00000616135.1:c.*626A= (MMACHC) ENSP00000478859.1:n.*626A=
NM_015506.2:c.*1807A= (MMACHC) NP_056321.2:n.*1807A=
NM_001330540.1:c.*1807A= (MMACHC) NP_001317469.1:n.*1807A=
XM_005270724.5:c.*1807A= (MMACHC) XP_005270781.1:n.*1807A=
NM_015506.3:c.*1807A= (MMACHC) MANE Select NP_056321.2:n.*1807A=
NM_001330540.2:c.*1807A= (MMACHC) NP_001317469.1:n.*1807A=