Canonical Allele Identifier: CA2335961483

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396131G= , CM000681.2:g.40396131G=	GRCh38
NC_000019.9:g.40902038G= , CM000681.1:g.40902038G=	GRCh37
NC_000019.8:g.45593878G=	NCBI36
NG_007979.1:g.22234C= , LRG_265:g.22234C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.2221C= MANE Select	ENSP00000326018.6:p.His741=
ENST00000673881.1:c.1804C=	ENSP00000501070.1:p.His602=
ENST00000674005.2:c.2506C=	ENSP00000501261.1:p.His836=
ENST00000674773.1:c.1804C=	ENSP00000502579.1:p.His602=
ENST00000675517.1:c.2096C=
ENST00000676076.1:c.2082C=
ENST00000676260.1:c.2183C=
ENST00000676316.1:c.2108C=
ENST00000291825.11:c.*2426C=	ENSP00000291825.6:n.*2426C=
ENST00000324001.7:c.2221C=	ENSP00000326018.6:p.His741=
NM_020956.2:c.*2426C= , LRG_265t1:c.*2426C=	NP_066007.1:n.*2426C=
NM_181882.2:c.2221C= , LRG_265t2:c.2221C=	NP_870998.2:p.His741=
XM_011527171.1:c.2221C=	XP_011525473.1:p.His741=
XM_011527171.2:c.2221C=	XP_011525473.1:p.His741=
XM_017027046.1:c.2119C=	XP_016882535.1:p.His707=
XM_017027047.1:c.2119C=	XP_016882536.1:p.His707=
NM_181882.3:c.2221C= MANE Select	NP_870998.2:p.His741=