Canonical Allele Identifier: CA10652456
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 329243
ClinVar RCV Id: RCV000367432
dbSNP Id: rs886054435

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40393814T>C , CM000681.2:g.40393814T>C GRCh38
NC_000019.9:g.40899721T>C , CM000681.1:g.40899721T>C GRCh37
NC_000019.8:g.45591561T>C NCBI36
NG_007979.1:g.24551A>G , LRG_265:g.24551A>G
NG_051224.1:g.1408A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000324001.8:c.*152A>G MANE Select ENSP00000326018.6:n.*152A>G
ENST00000673881.1:c.*152A>G ENSP00000501070.1:n.*152A>G
ENST00000674005.2:c.*152A>G ENSP00000501261.1:n.*152A>G
ENST00000674773.1:c.*152A>G ENSP00000502579.1:n.*152A>G
ENST00000676076.1:c.4399A>G
ENST00000676316.1:c.4425A>G
ENST00000291825.11:c.*4743A>G ENSP00000291825.6:n.*4743A>G
ENST00000324001.7:c.*152A>G ENSP00000326018.6:n.*152A>G
NM_020956.2:c.*4743A>G , LRG_265t1:c.*4743A>G NP_066007.1:n.*4743A>G
NM_181882.2:c.*152A>G , LRG_265t2:c.*152A>G NP_870998.2:n.*152A>G
XM_011527171.1:c.*152A>G XP_011525473.1:n.*152A>G
XM_011527171.2:c.*152A>G XP_011525473.1:n.*152A>G
XM_017027046.1:c.*152A>G XP_016882535.1:n.*152A>G
XM_017027047.1:c.*152A>G XP_016882536.1:n.*152A>G
NM_181882.3:c.*152A>G MANE Select NP_870998.2:n.*152A>G