Canonical Allele Identifier: CA405901695

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40403704A>G , CM000681.2:g.40403704A>G	GRCh38
NC_000019.9:g.40909611A>G , CM000681.1:g.40909611A>G	GRCh37
NC_000019.8:g.45601451A>G	NCBI36
NG_007979.1:g.14661T>C , LRG_265:g.14661T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_181882.3:c.184+2T>C MANE Select	NP_870998.2:n.184+2T>C
ENST00000324001.8:c.184+2T>C MANE Select	ENSP00000326018.6:n.184+2T>C
NM_020956.2:c.184+2T>C , LRG_265t1:c.184+2T>C	NP_066007.1:n.184+2T>C
NM_181882.2:c.184+2T>C , LRG_265t2:c.184+2T>C	NP_870998.2:n.184+2T>C
ENST00000291825.11:c.184+2T>C	ENSP00000291825.6:n.184+2T>C
ENST00000324001.7:c.184+2T>C	ENSP00000326018.6:n.184+2T>C
ENST00000673881.1:c.-234+2T>C	ENSP00000501070.1:n.-234+2T>C
ENST00000674005.2:c.469+2T>C	ENSP00000501261.1:n.469+2T>C
ENST00000674773.1:c.-37+2T>C	ENSP00000502579.1:n.-37+2T>C
ENST00000675300.1:c.157+2T>C	ENSP00000502008.1:n.157+2T>C
ENST00000676330.1:n.230+2T>C
XM_011527171.1:c.184+2T>C	XP_011525473.1:n.184+2T>C
XM_011527171.2:c.184+2T>C	XP_011525473.1:n.184+2T>C
XM_017027047.1:c.-49+2T>C	XP_016882536.1:n.-49+2T>C