Canonical Allele Identifier: CA339225

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394293_40394295del , CM000681.2:g.40394293_40394295del	GRCh38
NC_000019.9:g.40900200_40900202del , CM000681.1:g.40900200_40900202del	GRCh37
NC_000019.8:g.45592040_45592042del	NCBI36
NG_007979.1:g.24090_24092del , LRG_265:g.24090_24092del
NG_051224.1:g.947_949del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.4077_4079del MANE Select	ENSP00000326018.6:p.Glu1360del
ENST00000673881.1:c.3660_3662del	ENSP00000501070.1:p.Glu1221del
ENST00000674005.2:c.4362_4364del	ENSP00000501261.1:p.Glu1455del
ENST00000674773.1:c.3660_3662del	ENSP00000502579.1:p.Glu1221del
ENST00000675517.1:c.3952_3954del
ENST00000676076.1:c.3938_3940del
ENST00000676260.1:c.4039_4041del
ENST00000676316.1:c.3964_3966del
ENST00000291825.11:c.*4282_*4284del	ENSP00000291825.6:n.*4282_*4284del
ENST00000324001.7:c.4077_4079del	ENSP00000326018.6:p.Glu1360del
NM_020956.2:c.*4282_*4284del , LRG_265t1:c.*4282_*4284del	NP_066007.1:n.*4282_*4284del
NM_181882.2:c.4077_4079del , LRG_265t2:c.4077_4079del	NP_870998.2:p.Glu1360del
XM_011527171.1:c.4077_4079del	XP_011525473.1:p.Glu1360del
XM_011527171.2:c.4077_4079del	XP_011525473.1:p.Glu1360del
XM_017027046.1:c.3975_3977del	XP_016882535.1:p.Glu1326del
XM_017027047.1:c.3975_3977del	XP_016882536.1:p.Glu1326del
NM_181882.3:c.4077_4079del MANE Select	NP_870998.2:p.Glu1360del