Canonical Allele Identifier: CA1148454716

Gene: MMACHC PRDX1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45511037A= , CM000663.2:g.45511037A=	GRCh38
NC_000001.10:g.45976709A= , CM000663.1:g.45976709A=	GRCh37
NC_000001.9:g.45749296A=	NCBI36
NG_013378.1:g.15854A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401061.9:c.*1822A= (MMACHC) MANE Select	ENSP00000383840.4:n.*1822A=
ENST00000424390.2:c.*292T= (PRDX1)	ENSP00000389047.2:n.*292T=
ENST00000447184.6:c.*292T= (PRDX1)	ENSP00000407034.2:n.*292T=
ENST00000676549.1:c.*292T= (PRDX1)	ENSP00000503140.1:n.*292T=
ENST00000262746.5:c.*292T= (PRDX1)	ENSP00000262746.1:n.*292T=
ENST00000401061.8:c.*1822A= (MMACHC)	ENSP00000383840.4:n.*1822A=
ENST00000616135.1:c.*641A= (MMACHC)	ENSP00000478859.1:n.*641A=
NM_001202431.1:c.*292T= (PRDX1)	NP_001189360.1:n.*292T=
NM_002574.3:c.*292T= (PRDX1)	NP_002565.1:n.*292T=
NM_015506.2:c.*1822A= (MMACHC)	NP_056321.2:n.*1822A=
NM_181696.2:c.*292T= (PRDX1)	NP_859047.1:n.*292T=
NM_181697.2:c.*292T= (PRDX1)	NP_859048.1:n.*292T=
NM_001330540.1:c.*1822A= (MMACHC)	NP_001317469.1:n.*1822A=
XM_005270724.5:c.*1822A= (MMACHC)	XP_005270781.1:n.*1822A=
NM_015506.3:c.*1822A= (MMACHC) MANE Select	NP_056321.2:n.*1822A=
NM_001330540.2:c.*1822A= (MMACHC)	NP_001317469.1:n.*1822A=