Canonical Allele Identifier: CA522560281

Gene: PRDX1 MMACHC

Linked Data

• dbSNP Id: rs1259459655
• gnomAD v2: 1-45976990-C-T
• MyVariant Identifiers: chr1:g.45976990C>T (hg19) ; chr1:g.45511318C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45511318C>T , CM000663.2:g.45511318C>T	GRCh38
NC_000001.10:g.45976990C>T , CM000663.1:g.45976990C>T	GRCh37
NC_000001.9:g.45749577C>T	NCBI36
NG_013378.1:g.16135C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319248.13:c.*11G>A (PRDX1) MANE Select	ENSP00000361152.5:n.*11G>A
ENST00000401061.9:c.*2103C>T (MMACHC) MANE Select	ENSP00000383840.4:n.*2103C>T
ENST00000424390.2:c.*11G>A (PRDX1)	ENSP00000389047.2:n.*11G>A
ENST00000447184.6:c.*11G>A (PRDX1)	ENSP00000407034.2:n.*11G>A
ENST00000676549.1:c.*11G>A (PRDX1)	ENSP00000503140.1:n.*11G>A
ENST00000262746.5:c.*11G>A (PRDX1)	ENSP00000262746.1:n.*11G>A
ENST00000319248.12:c.*11G>A (PRDX1)	ENSP00000361152.5:n.*11G>A
ENST00000372079.1:c.*11G>A (PRDX1)	ENSP00000361150.1:n.*11G>A
ENST00000401061.8:c.*2103C>T (MMACHC)	ENSP00000383840.4:n.*2103C>T
NM_001202431.1:c.*11G>A (PRDX1)	NP_001189360.1:n.*11G>A
NM_002574.3:c.*11G>A (PRDX1)	NP_002565.1:n.*11G>A
NM_181696.2:c.*11G>A (PRDX1)	NP_859047.1:n.*11G>A
NM_181697.2:c.*11G>A (PRDX1)	NP_859048.1:n.*11G>A
NM_015506.3:c.*2103C>T (MMACHC) MANE Select	NP_056321.2:n.*2103C>T
NM_181697.3:c.*11G>A (PRDX1) MANE Select	NP_859048.1:n.*11G>A
NM_001330540.2:c.*2103C>T (MMACHC)	NP_001317469.1:n.*2103C>T
NM_001202431.2:c.*11G>A (PRDX1)	NP_001189360.1:n.*11G>A
NM_002574.4:c.*11G>A (PRDX1)	NP_002565.1:n.*11G>A
NM_181696.3:c.*11G>A (PRDX1)	NP_859047.1:n.*11G>A