Canonical Allele Identifier: CA405894242

Gene: PRX

Linked Data

• MyVariant Identifiers: chr19:g.40900927C>G (hg19) ; chr19:g.40395020C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40395020C>G , CM000681.2:g.40395020C>G	GRCh38
NC_000019.9:g.40900927C>G , CM000681.1:g.40900927C>G	GRCh37
NC_000019.8:g.45592767C>G	NCBI36
NG_007979.1:g.23345G>C , LRG_265:g.23345G>C
NG_051224.1:g.202G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.3332G>C MANE Select	ENSP00000326018.6:p.Arg1111Thr
ENST00000673881.1:c.2915G>C	ENSP00000501070.1:p.Arg972Thr
ENST00000674005.2:c.3617G>C	ENSP00000501261.1:p.Arg1206Thr
ENST00000674773.1:c.2915G>C	ENSP00000502579.1:p.Arg972Thr
ENST00000675517.1:c.3207G>C
ENST00000676076.1:c.3193G>C
ENST00000676260.1:c.3294G>C
ENST00000676316.1:c.3219G>C
ENST00000291825.11:c.*3537G>C	ENSP00000291825.6:n.*3537G>C
ENST00000324001.7:c.3332G>C	ENSP00000326018.6:p.Arg1111Thr
NM_020956.2:c.*3537G>C , LRG_265t1:c.*3537G>C	NP_066007.1:n.*3537G>C
NM_181882.2:c.3332G>C , LRG_265t2:c.3332G>C	NP_870998.2:p.Arg1111Thr
XM_011527171.1:c.3332G>C	XP_011525473.1:p.Arg1111Thr
XM_011527171.2:c.3332G>C	XP_011525473.1:p.Arg1111Thr
XM_017027046.1:c.3230G>C	XP_016882535.1:p.Arg1077Thr
XM_017027047.1:c.3230G>C	XP_016882536.1:p.Arg1077Thr
NM_181882.3:c.3332G>C MANE Select	NP_870998.2:p.Arg1111Thr