Canonical Allele Identifier: CA405894235
Gene: PRX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40395019C>A , CM000681.2:g.40395019C>A GRCh38
NC_000019.9:g.40900926C>A , CM000681.1:g.40900926C>A GRCh37
NC_000019.8:g.45592766C>A NCBI36
NG_007979.1:g.23346G>T , LRG_265:g.23346G>T
NG_051224.1:g.203G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000324001.8:c.3333G>T MANE Select ENSP00000326018.6:p.Arg1111Ser
ENST00000673881.1:c.2916G>T ENSP00000501070.1:p.Arg972Ser
ENST00000674005.2:c.3618G>T ENSP00000501261.1:p.Arg1206Ser
ENST00000674773.1:c.2916G>T ENSP00000502579.1:p.Arg972Ser
ENST00000675517.1:c.3208G>T
ENST00000676076.1:c.3194G>T
ENST00000676260.1:c.3295G>T
ENST00000676316.1:c.3220G>T
ENST00000291825.11:c.*3538G>T ENSP00000291825.6:n.*3538G>T
ENST00000324001.7:c.3333G>T ENSP00000326018.6:p.Arg1111Ser
NM_020956.2:c.*3538G>T , LRG_265t1:c.*3538G>T NP_066007.1:n.*3538G>T
NM_181882.2:c.3333G>T , LRG_265t2:c.3333G>T NP_870998.2:p.Arg1111Ser
XM_011527171.1:c.3333G>T XP_011525473.1:p.Arg1111Ser
XM_011527171.2:c.3333G>T XP_011525473.1:p.Arg1111Ser
XM_017027046.1:c.3231G>T XP_016882535.1:p.Arg1077Ser
XM_017027047.1:c.3231G>T XP_016882536.1:p.Arg1077Ser
NM_181882.3:c.3333G>T MANE Select NP_870998.2:p.Arg1111Ser