Canonical Allele Identifier: CA326899291
Gene: PRDX4 HGNC NCBI

Linked Data

dbSNP Id: rs795491
gnomAD v2: X-23698863-T-A
gnomAD v3: X-23680746-T-A
gnomAD v4: X-23680746-T-A
MyVariant Identifiers: chrX:g.23698863T>A (hg19) chrX:g.23680746T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.23680746T>A , CM000685.2:g.23680746T>A GRCh38
NC_000023.10:g.23698863T>A , CM000685.1:g.23698863T>A GRCh37
NC_000023.9:g.23608784T>A NCBI36
NG_012563.1:g.18219T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379341.9:c.599+1459T>A MANE Select ENSP00000368646.4:n.599+1459T>A
ENST00000379341.8:c.599+1459T>A ENSP00000368646.4:n.599+1459T>A
ENST00000439422.1:c.231+1459T>A
NM_006406.1:c.599+1459T>A NP_006397.1:n.599+1459T>A
XM_005274438.1:c.557+1459T>A XP_005274495.1:n.557+1459T>A
NM_006406.2:c.599+1459T>A MANE Select NP_006397.1:n.599+1459T>A
Search 100 bp 5'
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