Canonical Allele Identifier: CA9444195

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396555T>A , CM000681.2:g.40396555T>A	GRCh38
NC_000019.9:g.40902462T>A , CM000681.1:g.40902462T>A	GRCh37
NC_000019.8:g.45594302T>A	NCBI36
NG_007979.1:g.21810A>T , LRG_265:g.21810A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_181882.3:c.1797A>T MANE Select	NP_870998.2:p.Lys599Asn
ENST00000324001.8:c.1797A>T MANE Select	ENSP00000326018.6:p.Lys599Asn
NM_020956.2:c.*2002A>T , LRG_265t1:c.*2002A>T	NP_066007.1:n.*2002A>T
NM_181882.2:c.1797A>T , LRG_265t2:c.1797A>T	NP_870998.2:p.Lys599Asn
ENST00000291825.11:c.*2002A>T	ENSP00000291825.6:n.*2002A>T
ENST00000324001.7:c.1797A>T	ENSP00000326018.6:p.Lys599Asn
ENST00000673881.1:c.1380A>T	ENSP00000501070.1:p.Lys460Asn
ENST00000674005.2:c.2082A>T	ENSP00000501261.1:p.Lys694Asn
ENST00000674773.1:c.1380A>T	ENSP00000502579.1:p.Lys460Asn
ENST00000675517.1:c.1672A>T
ENST00000676076.1:c.1658A>T
ENST00000676260.1:c.1759A>T
ENST00000676316.1:c.1684A>T
XM_011527171.1:c.1797A>T	XP_011525473.1:p.Lys599Asn
XM_011527171.2:c.1797A>T	XP_011525473.1:p.Lys599Asn
XM_017027046.1:c.1695A>T	XP_016882535.1:p.Lys565Asn
XM_017027047.1:c.1695A>T	XP_016882536.1:p.Lys565Asn