Canonical Allele Identifier: CA405897320

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396401C>A , CM000681.2:g.40396401C>A	GRCh38
NC_000019.9:g.40902308C>A , CM000681.1:g.40902308C>A	GRCh37
NC_000019.8:g.45594148C>A	NCBI36
NG_007979.1:g.21964G>T , LRG_265:g.21964G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.1951G>T MANE Select	ENSP00000326018.6:p.Asp651Tyr
ENST00000673881.1:c.1534G>T	ENSP00000501070.1:p.Asp512Tyr
ENST00000674005.2:c.2236G>T	ENSP00000501261.1:p.Asp746Tyr
ENST00000674773.1:c.1534G>T	ENSP00000502579.1:p.Asp512Tyr
ENST00000675517.1:c.1826G>T
ENST00000676076.1:c.1812G>T
ENST00000676260.1:c.1913G>T
ENST00000676316.1:c.1838G>T
ENST00000291825.11:c.*2156G>T	ENSP00000291825.6:n.*2156G>T
ENST00000324001.7:c.1951G>T	ENSP00000326018.6:p.Asp651Tyr
NM_020956.2:c.*2156G>T , LRG_265t1:c.*2156G>T	NP_066007.1:n.*2156G>T
NM_181882.2:c.1951G>T , LRG_265t2:c.1951G>T	NP_870998.2:p.Asp651Tyr
XM_011527171.1:c.1951G>T	XP_011525473.1:p.Asp651Tyr
XM_011527171.2:c.1951G>T	XP_011525473.1:p.Asp651Tyr
XM_017027046.1:c.1849G>T	XP_016882535.1:p.Asp617Tyr
XM_017027047.1:c.1849G>T	XP_016882536.1:p.Asp617Tyr
NM_181882.3:c.1951G>T MANE Select	NP_870998.2:p.Asp651Tyr