Canonical Allele Identifier: CA2840627678

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40395949dup , CM000681.2:g.40395949dup	GRCh38
NC_000019.9:g.40901856dup , CM000681.1:g.40901856dup	GRCh37
NC_000019.8:g.45593696dup	NCBI36
NG_007979.1:g.22416dup , LRG_265:g.22416dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.2403dup MANE Select	ENSP00000326018.6:p.Pro802AlafsTer25
ENST00000673881.1:c.1986dup	ENSP00000501070.1:p.Pro663AlafsTer25
ENST00000674005.2:c.2688dup	ENSP00000501261.1:p.Pro897AlafsTer25
ENST00000674773.1:c.1986dup	ENSP00000502579.1:p.Pro663AlafsTer25
ENST00000675517.1:c.2278dup
ENST00000676076.1:c.2264dup
ENST00000676260.1:c.2365dup
ENST00000676316.1:c.2290dup
ENST00000291825.11:c.*2608dup	ENSP00000291825.6:n.*2608dup
ENST00000324001.7:c.2403dup	ENSP00000326018.6:p.Pro802AlafsTer25
NM_020956.2:c.*2608dup , LRG_265t1:c.*2608dup	NP_066007.1:n.*2608dup
NM_181882.2:c.2403dup , LRG_265t2:c.2403dup	NP_870998.2:p.Pro802AlafsTer25
XM_011527171.1:c.2403dup	XP_011525473.1:p.Pro802AlafsTer25
XM_011527171.2:c.2403dup	XP_011525473.1:p.Pro802AlafsTer25
XM_017027046.1:c.2301dup	XP_016882535.1:p.Pro768AlafsTer25
XM_017027047.1:c.2301dup	XP_016882536.1:p.Pro768AlafsTer25
NM_181882.3:c.2403dup MANE Select	NP_870998.2:p.Pro802AlafsTer25