Canonical Allele Identifier: CA405889473

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394022C>G , CM000681.2:g.40394022C>G	GRCh38
NC_000019.9:g.40899929C>G , CM000681.1:g.40899929C>G	GRCh37
NC_000019.8:g.45591769C>G	NCBI36
NG_007979.1:g.24343G>C , LRG_265:g.24343G>C
NG_051224.1:g.1200G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_181882.3:c.4330G>C MANE Select	NP_870998.2:p.Glu1444Gln
ENST00000324001.8:c.4330G>C MANE Select	ENSP00000326018.6:p.Glu1444Gln
NM_020956.2:c.*4535G>C , LRG_265t1:c.*4535G>C	NP_066007.1:n.*4535G>C
NM_181882.2:c.4330G>C , LRG_265t2:c.4330G>C	NP_870998.2:p.Glu1444Gln
ENST00000291825.11:c.*4535G>C	ENSP00000291825.6:n.*4535G>C
ENST00000324001.7:c.4330G>C	ENSP00000326018.6:p.Glu1444Gln
ENST00000673881.1:c.3913G>C	ENSP00000501070.1:p.Glu1305Gln
ENST00000674005.2:c.4615G>C	ENSP00000501261.1:p.Glu1539Gln
ENST00000674773.1:c.3913G>C	ENSP00000502579.1:p.Glu1305Gln
ENST00000675517.1:c.4205G>C
ENST00000676076.1:c.4191G>C
ENST00000676260.1:c.4292G>C
ENST00000676316.1:c.4217G>C
XM_011527171.1:c.4330G>C	XP_011525473.1:p.Glu1444Gln
XM_011527171.2:c.4330G>C	XP_011525473.1:p.Glu1444Gln
XM_017027046.1:c.4228G>C	XP_016882535.1:p.Glu1410Gln
XM_017027047.1:c.4228G>C	XP_016882536.1:p.Glu1410Gln