Canonical Allele Identifier: CA2335962031

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40397178_40397179delinsGA , CM000681.2:g.40397178_40397179delinsGA	GRCh38
NC_000019.9:g.40903085_40903086delinsGA , CM000681.1:g.40903085_40903086delinsGA	GRCh37
NC_000019.8:g.45594925_45594926delinsGA	NCBI36
NG_007979.1:g.21186_21187delinsTC , LRG_265:g.21186_21187delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000324001.8:c.1173_1174delinsTC MANE Select	ENSP00000326018.6:p.Leu391=
ENST00000673881.1:c.756_757delinsTC	ENSP00000501070.1:p.Leu252=
ENST00000674005.2:c.1458_1459delinsTC	ENSP00000501261.1:p.Leu486=
ENST00000674773.1:c.756_757delinsTC	ENSP00000502579.1:p.Leu252=
ENST00000675517.1:c.1048_1049delinsTC
ENST00000676076.1:c.1034_1035delinsTC
ENST00000676260.1:c.1135_1136delinsTC
ENST00000676316.1:c.1060_1061delinsTC
ENST00000291825.11:c.*1378_*1379delinsTC	ENSP00000291825.6:n.*1378_*1379delinsTC
ENST00000324001.7:c.1173_1174delinsTC	ENSP00000326018.6:p.Leu391=
NM_020956.2:c.*1378_*1379delinsTC , LRG_265t1:c.*1378_*1379delinsTC	NP_066007.1:n.*1378_*1379delinsTC
NM_181882.2:c.1173_1174delinsTC , LRG_265t2:c.1173_1174delinsTC	NP_870998.2:p.Leu391=
XM_011527171.1:c.1173_1174delinsTC	XP_011525473.1:p.Leu391=
XM_011527171.2:c.1173_1174delinsTC	XP_011525473.1:p.Leu391=
XM_017027046.1:c.1071_1072delinsTC	XP_016882535.1:p.Leu357=
XM_017027047.1:c.1071_1072delinsTC	XP_016882536.1:p.Leu357=
NM_181882.3:c.1173_1174delinsTC MANE Select	NP_870998.2:p.Leu391=