Canonical Allele Identifier: CA405894264

Gene: PRX

Linked Data

• MyVariant Identifiers: chr19:g.40900931C>T (hg19) ; chr19:g.40395024C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40395024C>T , CM000681.2:g.40395024C>T	GRCh38
NC_000019.9:g.40900931C>T , CM000681.1:g.40900931C>T	GRCh37
NC_000019.8:g.45592771C>T	NCBI36
NG_007979.1:g.23341G>A , LRG_265:g.23341G>A
NG_051224.1:g.198G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.3328G>A MANE Select	ENSP00000326018.6:p.Gly1110Arg
ENST00000673881.1:c.2911G>A	ENSP00000501070.1:p.Gly971Arg
ENST00000674005.2:c.3613G>A	ENSP00000501261.1:p.Gly1205Arg
ENST00000674773.1:c.2911G>A	ENSP00000502579.1:p.Gly971Arg
ENST00000675517.1:c.3203G>A
ENST00000676076.1:c.3189G>A
ENST00000676260.1:c.3290G>A
ENST00000676316.1:c.3215G>A
ENST00000291825.11:c.*3533G>A	ENSP00000291825.6:n.*3533G>A
ENST00000324001.7:c.3328G>A	ENSP00000326018.6:p.Gly1110Arg
NM_020956.2:c.*3533G>A , LRG_265t1:c.*3533G>A	NP_066007.1:n.*3533G>A
NM_181882.2:c.3328G>A , LRG_265t2:c.3328G>A	NP_870998.2:p.Gly1110Arg
XM_011527171.1:c.3328G>A	XP_011525473.1:p.Gly1110Arg
XM_011527171.2:c.3328G>A	XP_011525473.1:p.Gly1110Arg
XM_017027046.1:c.3226G>A	XP_016882535.1:p.Gly1076Arg
XM_017027047.1:c.3226G>A	XP_016882536.1:p.Gly1076Arg
NM_181882.3:c.3328G>A MANE Select	NP_870998.2:p.Gly1110Arg