Canonical Allele Identifier: CA2840627681

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396267dup , CM000681.2:g.40396267dup	GRCh38
NC_000019.9:g.40902174dup , CM000681.1:g.40902174dup	GRCh37
NC_000019.8:g.45594014dup	NCBI36
NG_007979.1:g.22099dup , LRG_265:g.22099dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.2086dup MANE Select	ENSP00000326018.6:p.Val696GlyfsTer3
ENST00000673881.1:c.1669dup	ENSP00000501070.1:p.Val557GlyfsTer3
ENST00000674005.2:c.2371dup	ENSP00000501261.1:p.Val791GlyfsTer3
ENST00000674773.1:c.1669dup	ENSP00000502579.1:p.Val557GlyfsTer3
ENST00000675517.1:c.1961dup
ENST00000676076.1:c.1947dup
ENST00000676260.1:c.2048dup
ENST00000676316.1:c.1973dup
ENST00000291825.11:c.*2291dup	ENSP00000291825.6:n.*2291dup
ENST00000324001.7:c.2086dup	ENSP00000326018.6:p.Val696GlyfsTer3
NM_020956.2:c.*2291dup , LRG_265t1:c.*2291dup	NP_066007.1:n.*2291dup
NM_181882.2:c.2086dup , LRG_265t2:c.2086dup	NP_870998.2:p.Val696GlyfsTer3
XM_011527171.1:c.2086dup	XP_011525473.1:p.Val696GlyfsTer3
XM_011527171.2:c.2086dup	XP_011525473.1:p.Val696GlyfsTer3
XM_017027046.1:c.1984dup	XP_016882535.1:p.Val662GlyfsTer3
XM_017027047.1:c.1984dup	XP_016882536.1:p.Val662GlyfsTer3
NM_181882.3:c.2086dup MANE Select	NP_870998.2:p.Val696GlyfsTer3