Canonical Allele Identifier: CA2645392708

Gene: MMACHC PRDX1

Linked Data

• gnomAD v4: 1-45511013-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45511013G>T , CM000663.2:g.45511013G>T	GRCh38
NC_000001.10:g.45976685G>T , CM000663.1:g.45976685G>T	GRCh37
NC_000001.9:g.45749272G>T	NCBI36
NG_013378.1:g.15830G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401061.9:c.*1798G>T (MMACHC) MANE Select	ENSP00000383840.4:n.*1798G>T
ENST00000424390.2:c.*316C>A (PRDX1)	ENSP00000389047.2:n.*316C>A
ENST00000447184.6:c.*316C>A (PRDX1)	ENSP00000407034.2:n.*316C>A
ENST00000676549.1:c.*316C>A (PRDX1)	ENSP00000503140.1:n.*316C>A
ENST00000401061.8:c.*1798G>T (MMACHC)	ENSP00000383840.4:n.*1798G>T
ENST00000616135.1:c.*617G>T (MMACHC)	ENSP00000478859.1:n.*617G>T
NM_015506.2:c.*1798G>T (MMACHC)	NP_056321.2:n.*1798G>T
NM_001330540.1:c.*1798G>T (MMACHC)	NP_001317469.1:n.*1798G>T
XM_005270724.5:c.*1798G>T (MMACHC)	XP_005270781.1:n.*1798G>T
NM_015506.3:c.*1798G>T (MMACHC) MANE Select	NP_056321.2:n.*1798G>T
NM_001330540.2:c.*1798G>T (MMACHC)	NP_001317469.1:n.*1798G>T