Canonical Allele Identifier: CA2839123812

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40395020dup , CM000681.2:g.40395020dup	GRCh38
NC_000019.9:g.40900927dup , CM000681.1:g.40900927dup	GRCh37
NC_000019.8:g.45592767dup	NCBI36
NG_007979.1:g.23347dup , LRG_265:g.23347dup
NG_051224.1:g.204dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.3334dup MANE Select	ENSP00000326018.6:p.Ala1112GlyfsTer26
ENST00000673881.1:c.2917dup	ENSP00000501070.1:p.Ala973GlyfsTer26
ENST00000674005.2:c.3619dup	ENSP00000501261.1:p.Ala1207GlyfsTer26
ENST00000674773.1:c.2917dup	ENSP00000502579.1:p.Ala973GlyfsTer26
ENST00000675517.1:c.3209dup
ENST00000676076.1:c.3195dup
ENST00000676260.1:c.3296dup
ENST00000676316.1:c.3221dup
ENST00000291825.11:c.*3539dup	ENSP00000291825.6:n.*3539dup
ENST00000324001.7:c.3334dup	ENSP00000326018.6:p.Ala1112GlyfsTer26
NM_020956.2:c.*3539dup , LRG_265t1:c.*3539dup	NP_066007.1:n.*3539dup
NM_181882.2:c.3334dup , LRG_265t2:c.3334dup	NP_870998.2:p.Ala1112GlyfsTer26
XM_011527171.1:c.3334dup	XP_011525473.1:p.Ala1112GlyfsTer26
XM_011527171.2:c.3334dup	XP_011525473.1:p.Ala1112GlyfsTer26
XM_017027046.1:c.3232dup	XP_016882535.1:p.Ala1078GlyfsTer26
XM_017027047.1:c.3232dup	XP_016882536.1:p.Ala1078GlyfsTer26
NM_181882.3:c.3334dup MANE Select	NP_870998.2:p.Ala1112GlyfsTer26