Canonical Allele Identifier: CA2840627679

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40395952dup , CM000681.2:g.40395952dup	GRCh38
NC_000019.9:g.40901859dup , CM000681.1:g.40901859dup	GRCh37
NC_000019.8:g.45593699dup	NCBI36
NG_007979.1:g.22413dup , LRG_265:g.22413dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.2400dup MANE Select	ENSP00000326018.6:p.Met801AspfsTer26
ENST00000673881.1:c.1983dup	ENSP00000501070.1:p.Met662AspfsTer26
ENST00000674005.2:c.2685dup	ENSP00000501261.1:p.Met896AspfsTer26
ENST00000674773.1:c.1983dup	ENSP00000502579.1:p.Met662AspfsTer26
ENST00000675517.1:c.2275dup
ENST00000676076.1:c.2261dup
ENST00000676260.1:c.2362dup
ENST00000676316.1:c.2287dup
ENST00000291825.11:c.*2605dup	ENSP00000291825.6:n.*2605dup
ENST00000324001.7:c.2400dup	ENSP00000326018.6:p.Met801AspfsTer26
NM_020956.2:c.*2605dup , LRG_265t1:c.*2605dup	NP_066007.1:n.*2605dup
NM_181882.2:c.2400dup , LRG_265t2:c.2400dup	NP_870998.2:p.Met801AspfsTer26
XM_011527171.1:c.2400dup	XP_011525473.1:p.Met801AspfsTer26
XM_011527171.2:c.2400dup	XP_011525473.1:p.Met801AspfsTer26
XM_017027046.1:c.2298dup	XP_016882535.1:p.Met767AspfsTer26
XM_017027047.1:c.2298dup	XP_016882536.1:p.Met767AspfsTer26
NM_181882.3:c.2400dup MANE Select	NP_870998.2:p.Met801AspfsTer26