Canonical Allele Identifier: CA2838616128

Gene: PRX

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.3413del MANE Select	ENSP00000326018.6:p.Gly1138AlafsTer6
ENST00000673881.1:c.2996del	ENSP00000501070.1:p.Gly999AlafsTer6
ENST00000674005.2:c.3698del	ENSP00000501261.1:p.Gly1233AlafsTer6
ENST00000674773.1:c.2996del	ENSP00000502579.1:p.Gly999AlafsTer6
ENST00000675517.1:c.3288del
ENST00000676076.1:c.3274del
ENST00000676260.1:c.3375del
ENST00000676316.1:c.3300del
ENST00000291825.11:c.*3618del	ENSP00000291825.6:n.*3618del
ENST00000324001.7:c.3413del	ENSP00000326018.6:p.Gly1138AlafsTer6
NM_020956.2:c.*3618del , LRG_265t1:c.*3618del	NP_066007.1:n.*3618del
NM_181882.2:c.3413del , LRG_265t2:c.3413del	NP_870998.2:p.Gly1138AlafsTer6
XM_011527171.1:c.3413del	XP_011525473.1:p.Gly1138AlafsTer6
XM_011527171.2:c.3413del	XP_011525473.1:p.Gly1138AlafsTer6
XM_017027046.1:c.3311del	XP_016882535.1:p.Gly1104AlafsTer6
XM_017027047.1:c.3311del	XP_016882536.1:p.Gly1104AlafsTer6
NM_181882.3:c.3413del MANE Select	NP_870998.2:p.Gly1138AlafsTer6