Canonical Allele Identifier: CA2839145289

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40395967del , CM000681.2:g.40395967del	GRCh38
NC_000019.9:g.40901874del , CM000681.1:g.40901874del	GRCh37
NC_000019.8:g.45593714del	NCBI36
NG_007979.1:g.22399del , LRG_265:g.22399del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.2386del MANE Select	ENSP00000326018.6:p.Glu796AsnfsTer9
ENST00000673881.1:c.1969del	ENSP00000501070.1:p.Glu657AsnfsTer9
ENST00000674005.2:c.2671del	ENSP00000501261.1:p.Glu891AsnfsTer9
ENST00000674773.1:c.1969del	ENSP00000502579.1:p.Glu657AsnfsTer9
ENST00000675517.1:c.2261del
ENST00000676076.1:c.2247del
ENST00000676260.1:c.2348del
ENST00000676316.1:c.2273del
ENST00000291825.11:c.*2591del	ENSP00000291825.6:n.*2591del
ENST00000324001.7:c.2386del	ENSP00000326018.6:p.Glu796AsnfsTer9
NM_020956.2:c.*2591del , LRG_265t1:c.*2591del	NP_066007.1:n.*2591del
NM_181882.2:c.2386del , LRG_265t2:c.2386del	NP_870998.2:p.Glu796AsnfsTer9
XM_011527171.1:c.2386del	XP_011525473.1:p.Glu796AsnfsTer9
XM_011527171.2:c.2386del	XP_011525473.1:p.Glu796AsnfsTer9
XM_017027046.1:c.2284del	XP_016882535.1:p.Glu762AsnfsTer9
XM_017027047.1:c.2284del	XP_016882536.1:p.Glu762AsnfsTer9
NM_181882.3:c.2386del MANE Select	NP_870998.2:p.Glu796AsnfsTer9