Canonical Allele Identifier: CA2839544677

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394941dup , CM000681.2:g.40394941dup	GRCh38
NC_000019.9:g.40900848dup , CM000681.1:g.40900848dup	GRCh37
NC_000019.8:g.45592688dup	NCBI36
NG_007979.1:g.23426dup , LRG_265:g.23426dup
NG_051224.1:g.283dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.3413dup MANE Select	ENSP00000326018.6:p.His1139ProfsTer2
ENST00000673881.1:c.2996dup	ENSP00000501070.1:p.His1000ProfsTer2
ENST00000674005.2:c.3698dup	ENSP00000501261.1:p.His1234ProfsTer2
ENST00000674773.1:c.2996dup	ENSP00000502579.1:p.His1000ProfsTer2
ENST00000675517.1:c.3288dup
ENST00000676076.1:c.3274dup
ENST00000676260.1:c.3375dup
ENST00000676316.1:c.3300dup
ENST00000291825.11:c.*3618dup	ENSP00000291825.6:n.*3618dup
ENST00000324001.7:c.3413dup	ENSP00000326018.6:p.His1139ProfsTer2
NM_020956.2:c.*3618dup , LRG_265t1:c.*3618dup	NP_066007.1:n.*3618dup
NM_181882.2:c.3413dup , LRG_265t2:c.3413dup	NP_870998.2:p.His1139ProfsTer2
XM_011527171.1:c.3413dup	XP_011525473.1:p.His1139ProfsTer2
XM_011527171.2:c.3413dup	XP_011525473.1:p.His1139ProfsTer2
XM_017027046.1:c.3311dup	XP_016882535.1:p.His1105ProfsTer2
XM_017027047.1:c.3311dup	XP_016882536.1:p.His1105ProfsTer2
NM_181882.3:c.3413dup MANE Select	NP_870998.2:p.His1139ProfsTer2