Canonical Allele Identifier: CA405891709

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394451C>G , CM000681.2:g.40394451C>G	GRCh38
NC_000019.9:g.40900358C>G , CM000681.1:g.40900358C>G	GRCh37
NC_000019.8:g.45592198C>G	NCBI36
NG_007979.1:g.23914G>C , LRG_265:g.23914G>C
NG_051224.1:g.771G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_181882.3:c.3901G>C MANE Select	NP_870998.2:p.Gly1301Arg
ENST00000324001.8:c.3901G>C MANE Select	ENSP00000326018.6:p.Gly1301Arg
NM_020956.2:c.*4106G>C , LRG_265t1:c.*4106G>C	NP_066007.1:n.*4106G>C
NM_181882.2:c.3901G>C , LRG_265t2:c.3901G>C	NP_870998.2:p.Gly1301Arg
ENST00000291825.11:c.*4106G>C	ENSP00000291825.6:n.*4106G>C
ENST00000324001.7:c.3901G>C	ENSP00000326018.6:p.Gly1301Arg
ENST00000673881.1:c.3484G>C	ENSP00000501070.1:p.Gly1162Arg
ENST00000674005.2:c.4186G>C	ENSP00000501261.1:p.Gly1396Arg
ENST00000674773.1:c.3484G>C	ENSP00000502579.1:p.Gly1162Arg
ENST00000675517.1:c.3776G>C
ENST00000676076.1:c.3762G>C
ENST00000676260.1:c.3863G>C
ENST00000676316.1:c.3788G>C
XM_011527171.1:c.3901G>C	XP_011525473.1:p.Gly1301Arg
XM_011527171.2:c.3901G>C	XP_011525473.1:p.Gly1301Arg
XM_017027046.1:c.3799G>C	XP_016882535.1:p.Gly1267Arg
XM_017027047.1:c.3799G>C	XP_016882536.1:p.Gly1267Arg