Canonical Allele Identifier: CA405902026

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40407905C>A , CM000681.2:g.40407905C>A	GRCh38
NC_000019.9:g.40913812C>A , CM000681.1:g.40913812C>A	GRCh37
NC_000019.8:g.45605652C>A	NCBI36
NG_007979.1:g.10460G>T , LRG_265:g.10460G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_181882.3:c.27+1G>T MANE Select	NP_870998.2:n.27+1G>T
ENST00000324001.8:c.27+1G>T MANE Select	ENSP00000326018.6:n.27+1G>T
NM_020956.2:c.27+1G>T , LRG_265t1:c.27+1G>T	NP_066007.1:n.27+1G>T
NM_181882.2:c.27+1G>T , LRG_265t2:c.27+1G>T	NP_870998.2:n.27+1G>T
ENST00000291825.11:c.27+1G>T	ENSP00000291825.6:n.27+1G>T
ENST00000324001.7:c.27+1G>T	ENSP00000326018.6:n.27+1G>T
ENST00000599513.1:n.212+1G>T
ENST00000674005.2:c.312+1G>T	ENSP00000501261.1:n.312+1G>T
ENST00000674781.1:n.126+1G>T
ENST00000674912.1:n.126+1G>T
ENST00000675541.1:n.126+1G>T
ENST00000676344.1:n.126+1G>T
XM_011527171.1:c.27+1G>T	XP_011525473.1:n.27+1G>T
XM_011527171.2:c.27+1G>T	XP_011525473.1:n.27+1G>T