Canonical Allele Identifier: CA9443665

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394146G>A , CM000681.2:g.40394146G>A	GRCh38
NC_000019.9:g.40900053G>A , CM000681.1:g.40900053G>A	GRCh37
NC_000019.8:g.45591893G>A	NCBI36
NG_007979.1:g.24219C>T , LRG_265:g.24219C>T
NG_051224.1:g.1076C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_181882.3:c.4206C>T MANE Select	NP_870998.2:p.Pro1402=
ENST00000324001.8:c.4206C>T MANE Select	ENSP00000326018.6:p.Pro1402=
NM_020956.2:c.*4411C>T , LRG_265t1:c.*4411C>T	NP_066007.1:n.*4411C>T
NM_181882.2:c.4206C>T , LRG_265t2:c.4206C>T	NP_870998.2:p.Pro1402=
ENST00000291825.11:c.*4411C>T	ENSP00000291825.6:n.*4411C>T
ENST00000324001.7:c.4206C>T	ENSP00000326018.6:p.Pro1402=
ENST00000673881.1:c.3789C>T	ENSP00000501070.1:p.Pro1263=
ENST00000674005.2:c.4491C>T	ENSP00000501261.1:p.Pro1497=
ENST00000674773.1:c.3789C>T	ENSP00000502579.1:p.Pro1263=
ENST00000675517.1:c.4081C>T
ENST00000676076.1:c.4067C>T
ENST00000676260.1:c.4168C>T
ENST00000676316.1:c.4093C>T
XM_011527171.1:c.4206C>T	XP_011525473.1:p.Pro1402=
XM_011527171.2:c.4206C>T	XP_011525473.1:p.Pro1402=
XM_017027046.1:c.4104C>T	XP_016882535.1:p.Pro1368=
XM_017027047.1:c.4104C>T	XP_016882536.1:p.Pro1368=