Canonical Allele Identifier: CA405895545

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40395548T>G , CM000681.2:g.40395548T>G	GRCh38
NC_000019.9:g.40901455T>G , CM000681.1:g.40901455T>G	GRCh37
NC_000019.8:g.45593295T>G	NCBI36
NG_007979.1:g.22817A>C , LRG_265:g.22817A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_181882.3:c.2804A>C MANE Select	NP_870998.2:p.Lys935Thr
ENST00000324001.8:c.2804A>C MANE Select	ENSP00000326018.6:p.Lys935Thr
NM_020956.2:c.*3009A>C , LRG_265t1:c.*3009A>C	NP_066007.1:n.*3009A>C
NM_181882.2:c.2804A>C , LRG_265t2:c.2804A>C	NP_870998.2:p.Lys935Thr
ENST00000291825.11:c.*3009A>C	ENSP00000291825.6:n.*3009A>C
ENST00000324001.7:c.2804A>C	ENSP00000326018.6:p.Lys935Thr
ENST00000673881.1:c.2387A>C	ENSP00000501070.1:p.Lys796Thr
ENST00000674005.2:c.3089A>C	ENSP00000501261.1:p.Lys1030Thr
ENST00000674773.1:c.2387A>C	ENSP00000502579.1:p.Lys796Thr
ENST00000675517.1:c.2679A>C
ENST00000676076.1:c.2665A>C
ENST00000676260.1:c.2766A>C
ENST00000676316.1:c.2691A>C
XM_011527171.1:c.2804A>C	XP_011525473.1:p.Lys935Thr
XM_011527171.2:c.2804A>C	XP_011525473.1:p.Lys935Thr
XM_017027046.1:c.2702A>C	XP_016882535.1:p.Lys901Thr
XM_017027047.1:c.2702A>C	XP_016882536.1:p.Lys901Thr