Canonical Allele Identifier: CA2335960929

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394952C= , CM000681.2:g.40394952C=	GRCh38
NC_000019.9:g.40900859C= , CM000681.1:g.40900859C=	GRCh37
NC_000019.8:g.45592699C=	NCBI36
NG_007979.1:g.23413G= , LRG_265:g.23413G=
NG_051224.1:g.270G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.3400G= MANE Select	ENSP00000326018.6:p.Val1134=
ENST00000673881.1:c.2983G=	ENSP00000501070.1:p.Val995=
ENST00000674005.2:c.3685G=	ENSP00000501261.1:p.Val1229=
ENST00000674773.1:c.2983G=	ENSP00000502579.1:p.Val995=
ENST00000675517.1:c.3275G=
ENST00000676076.1:c.3261G=
ENST00000676260.1:c.3362G=
ENST00000676316.1:c.3287G=
ENST00000291825.11:c.*3605G=	ENSP00000291825.6:n.*3605G=
ENST00000324001.7:c.3400G=	ENSP00000326018.6:p.Val1134=
NM_020956.2:c.*3605G= , LRG_265t1:c.*3605G=	NP_066007.1:n.*3605G=
NM_181882.2:c.3400G= , LRG_265t2:c.3400G=	NP_870998.2:p.Val1134=
XM_011527171.1:c.3400G=	XP_011525473.1:p.Val1134=
XM_011527171.2:c.3400G=	XP_011525473.1:p.Val1134=
XM_017027046.1:c.3298G=	XP_016882535.1:p.Val1100=
XM_017027047.1:c.3298G=	XP_016882536.1:p.Val1100=
NM_181882.3:c.3400G= MANE Select	NP_870998.2:p.Val1134=