Canonical Allele Identifier: CA405893528
Gene: PRX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40394874A>G , CM000681.2:g.40394874A>G GRCh38
NC_000019.9:g.40900781A>G , CM000681.1:g.40900781A>G GRCh37
NC_000019.8:g.45592621A>G NCBI36
NG_007979.1:g.23491T>C , LRG_265:g.23491T>C
NG_051224.1:g.348T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000324001.8:c.3478T>C MANE Select ENSP00000326018.6:p.Phe1160Leu
ENST00000673881.1:c.3061T>C ENSP00000501070.1:p.Phe1021Leu
ENST00000674005.2:c.3763T>C ENSP00000501261.1:p.Phe1255Leu
ENST00000674773.1:c.3061T>C ENSP00000502579.1:p.Phe1021Leu
ENST00000675517.1:c.3353T>C
ENST00000676076.1:c.3339T>C
ENST00000676260.1:c.3440T>C
ENST00000676316.1:c.3365T>C
ENST00000291825.11:c.*3683T>C ENSP00000291825.6:n.*3683T>C
ENST00000324001.7:c.3478T>C ENSP00000326018.6:p.Phe1160Leu
NM_020956.2:c.*3683T>C , LRG_265t1:c.*3683T>C NP_066007.1:n.*3683T>C
NM_181882.2:c.3478T>C , LRG_265t2:c.3478T>C NP_870998.2:p.Phe1160Leu
XM_011527171.1:c.3478T>C XP_011525473.1:p.Phe1160Leu
XM_011527171.2:c.3478T>C XP_011525473.1:p.Phe1160Leu
XM_017027046.1:c.3376T>C XP_016882535.1:p.Phe1126Leu
XM_017027047.1:c.3376T>C XP_016882536.1:p.Phe1126Leu
NM_181882.3:c.3478T>C MANE Select NP_870998.2:p.Phe1160Leu