Canonical Allele Identifier: CA405900032

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40397745G>A , CM000681.2:g.40397745G>A	GRCh38
NC_000019.9:g.40903652G>A , CM000681.1:g.40903652G>A	GRCh37
NC_000019.8:g.45595492G>A	NCBI36
NG_007979.1:g.20620C>T , LRG_265:g.20620C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_181882.3:c.607C>T MANE Select	NP_870998.2:p.Gln203Ter
ENST00000324001.8:c.607C>T MANE Select	ENSP00000326018.6:p.Gln203Ter
NM_020956.2:c.*812C>T , LRG_265t1:c.*812C>T	NP_066007.1:n.*812C>T
NM_181882.2:c.607C>T , LRG_265t2:c.607C>T	NP_870998.2:p.Gln203Ter
ENST00000291825.11:c.*812C>T	ENSP00000291825.6:n.*812C>T
ENST00000324001.7:c.607C>T	ENSP00000326018.6:p.Gln203Ter
ENST00000673881.1:c.190C>T	ENSP00000501070.1:p.Gln64Ter
ENST00000674005.2:c.892C>T	ENSP00000501261.1:p.Gln298Ter
ENST00000674773.1:c.190C>T	ENSP00000502579.1:p.Gln64Ter
ENST00000675517.1:c.482C>T
ENST00000676076.1:c.468C>T
ENST00000676260.1:c.569C>T
ENST00000676316.1:c.494C>T
XM_011527171.1:c.607C>T	XP_011525473.1:p.Gln203Ter
XM_011527171.2:c.607C>T	XP_011525473.1:p.Gln203Ter
XM_017027046.1:c.505C>T	XP_016882535.1:p.Gln169Ter
XM_017027047.1:c.505C>T	XP_016882536.1:p.Gln169Ter