Canonical Allele Identifier: CA405894098

Gene: PRX

Linked Data

• dbSNP Id: rs1240103185
• COSMIC: COSM3823118
• MyVariant Identifiers: chr19:g.40900900C>T (hg19) ; chr19:g.40394993C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394993C>T , CM000681.2:g.40394993C>T	GRCh38
NC_000019.9:g.40900900C>T , CM000681.1:g.40900900C>T	GRCh37
NC_000019.8:g.45592740C>T	NCBI36
NG_007979.1:g.23372G>A , LRG_265:g.23372G>A
NG_051224.1:g.229G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.3359G>A MANE Select	ENSP00000326018.6:p.Gly1120Glu
ENST00000673881.1:c.2942G>A	ENSP00000501070.1:p.Gly981Glu
ENST00000674005.2:c.3644G>A	ENSP00000501261.1:p.Gly1215Glu
ENST00000674773.1:c.2942G>A	ENSP00000502579.1:p.Gly981Glu
ENST00000675517.1:c.3234G>A
ENST00000676076.1:c.3220G>A
ENST00000676260.1:c.3321G>A
ENST00000676316.1:c.3246G>A
ENST00000291825.11:c.*3564G>A	ENSP00000291825.6:n.*3564G>A
ENST00000324001.7:c.3359G>A	ENSP00000326018.6:p.Gly1120Glu
NM_020956.2:c.*3564G>A , LRG_265t1:c.*3564G>A	NP_066007.1:n.*3564G>A
NM_181882.2:c.3359G>A , LRG_265t2:c.3359G>A	NP_870998.2:p.Gly1120Glu
XM_011527171.1:c.3359G>A	XP_011525473.1:p.Gly1120Glu
XM_011527171.2:c.3359G>A	XP_011525473.1:p.Gly1120Glu
XM_017027046.1:c.3257G>A	XP_016882535.1:p.Gly1086Glu
XM_017027047.1:c.3257G>A	XP_016882536.1:p.Gly1086Glu
NM_181882.3:c.3359G>A MANE Select	NP_870998.2:p.Gly1120Glu