Canonical Allele Identifier: CA405892600

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394649C>A , CM000681.2:g.40394649C>A	GRCh38
NC_000019.9:g.40900556C>A , CM000681.1:g.40900556C>A	GRCh37
NC_000019.8:g.45592396C>A	NCBI36
NG_007979.1:g.23716G>T , LRG_265:g.23716G>T
NG_051224.1:g.573G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_181882.3:c.3703G>T MANE Select	NP_870998.2:p.Glu1235Ter
ENST00000324001.8:c.3703G>T MANE Select	ENSP00000326018.6:p.Glu1235Ter
NM_020956.2:c.*3908G>T , LRG_265t1:c.*3908G>T	NP_066007.1:n.*3908G>T
NM_181882.2:c.3703G>T , LRG_265t2:c.3703G>T	NP_870998.2:p.Glu1235Ter
ENST00000291825.11:c.*3908G>T	ENSP00000291825.6:n.*3908G>T
ENST00000324001.7:c.3703G>T	ENSP00000326018.6:p.Glu1235Ter
ENST00000673881.1:c.3286G>T	ENSP00000501070.1:p.Glu1096Ter
ENST00000674005.2:c.3988G>T	ENSP00000501261.1:p.Glu1330Ter
ENST00000674773.1:c.3286G>T	ENSP00000502579.1:p.Glu1096Ter
ENST00000675517.1:c.3578G>T
ENST00000676076.1:c.3564G>T
ENST00000676260.1:c.3665G>T
ENST00000676316.1:c.3590G>T
XM_011527171.1:c.3703G>T	XP_011525473.1:p.Glu1235Ter
XM_011527171.2:c.3703G>T	XP_011525473.1:p.Glu1235Ter
XM_017027046.1:c.3601G>T	XP_016882535.1:p.Glu1201Ter
XM_017027047.1:c.3601G>T	XP_016882536.1:p.Glu1201Ter