Canonical Allele Identifier: CA9443727

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394389C>T , CM000681.2:g.40394389C>T	GRCh38
NC_000019.9:g.40900296C>T , CM000681.1:g.40900296C>T	GRCh37
NC_000019.8:g.45592136C>T	NCBI36
NG_007979.1:g.23976G>A , LRG_265:g.23976G>A
NG_051224.1:g.833G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_181882.3:c.3963G>A MANE Select	NP_870998.2:p.Glu1321=
ENST00000324001.8:c.3963G>A MANE Select	ENSP00000326018.6:p.Glu1321=
NM_020956.2:c.*4168G>A , LRG_265t1:c.*4168G>A	NP_066007.1:n.*4168G>A
NM_181882.2:c.3963G>A , LRG_265t2:c.3963G>A	NP_870998.2:p.Glu1321=
ENST00000291825.11:c.*4168G>A	ENSP00000291825.6:n.*4168G>A
ENST00000324001.7:c.3963G>A	ENSP00000326018.6:p.Glu1321=
ENST00000673881.1:c.3546G>A	ENSP00000501070.1:p.Glu1182=
ENST00000674005.2:c.4248G>A	ENSP00000501261.1:p.Glu1416=
ENST00000674773.1:c.3546G>A	ENSP00000502579.1:p.Glu1182=
ENST00000675517.1:c.3838G>A
ENST00000676076.1:c.3824G>A
ENST00000676260.1:c.3925G>A
ENST00000676316.1:c.3850G>A
XM_011527171.1:c.3963G>A	XP_011525473.1:p.Glu1321=
XM_011527171.2:c.3963G>A	XP_011525473.1:p.Glu1321=
XM_017027046.1:c.3861G>A	XP_016882535.1:p.Glu1287=
XM_017027047.1:c.3861G>A	XP_016882536.1:p.Glu1287=