Canonical Allele Identifier: CA405894060

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394987T>C , CM000681.2:g.40394987T>C	GRCh38
NC_000019.9:g.40900894T>C , CM000681.1:g.40900894T>C	GRCh37
NC_000019.8:g.45592734T>C	NCBI36
NG_007979.1:g.23378A>G , LRG_265:g.23378A>G
NG_051224.1:g.235A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_181882.3:c.3365A>G MANE Select	NP_870998.2:p.Gln1122Arg
ENST00000324001.8:c.3365A>G MANE Select	ENSP00000326018.6:p.Gln1122Arg
NM_020956.2:c.*3570A>G , LRG_265t1:c.*3570A>G	NP_066007.1:n.*3570A>G
NM_181882.2:c.3365A>G , LRG_265t2:c.3365A>G	NP_870998.2:p.Gln1122Arg
ENST00000291825.11:c.*3570A>G	ENSP00000291825.6:n.*3570A>G
ENST00000324001.7:c.3365A>G	ENSP00000326018.6:p.Gln1122Arg
ENST00000673881.1:c.2948A>G	ENSP00000501070.1:p.Gln983Arg
ENST00000674005.2:c.3650A>G	ENSP00000501261.1:p.Gln1217Arg
ENST00000674773.1:c.2948A>G	ENSP00000502579.1:p.Gln983Arg
ENST00000675517.1:c.3240A>G
ENST00000676076.1:c.3226A>G
ENST00000676260.1:c.3327A>G
ENST00000676316.1:c.3252A>G
XM_011527171.1:c.3365A>G	XP_011525473.1:p.Gln1122Arg
XM_011527171.2:c.3365A>G	XP_011525473.1:p.Gln1122Arg
XM_017027046.1:c.3263A>G	XP_016882535.1:p.Gln1088Arg
XM_017027047.1:c.3263A>G	XP_016882536.1:p.Gln1088Arg