Canonical Allele Identifier: CA2335960893

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394883G= , CM000681.2:g.40394883G=	GRCh38
NC_000019.9:g.40900790G= , CM000681.1:g.40900790G=	GRCh37
NC_000019.8:g.45592630G=	NCBI36
NG_007979.1:g.23482C= , LRG_265:g.23482C=
NG_051224.1:g.339C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.3469C= MANE Select	ENSP00000326018.6:p.Leu1157=
ENST00000673881.1:c.3052C=	ENSP00000501070.1:p.Leu1018=
ENST00000674005.2:c.3754C=	ENSP00000501261.1:p.Leu1252=
ENST00000674773.1:c.3052C=	ENSP00000502579.1:p.Leu1018=
ENST00000675517.1:c.3344C=
ENST00000676076.1:c.3330C=
ENST00000676260.1:c.3431C=
ENST00000676316.1:c.3356C=
ENST00000291825.11:c.*3674C=	ENSP00000291825.6:n.*3674C=
ENST00000324001.7:c.3469C=	ENSP00000326018.6:p.Leu1157=
NM_020956.2:c.*3674C= , LRG_265t1:c.*3674C=	NP_066007.1:n.*3674C=
NM_181882.2:c.3469C= , LRG_265t2:c.3469C=	NP_870998.2:p.Leu1157=
XM_011527171.1:c.3469C=	XP_011525473.1:p.Leu1157=
XM_011527171.2:c.3469C=	XP_011525473.1:p.Leu1157=
XM_017027046.1:c.3367C=	XP_016882535.1:p.Leu1123=
XM_017027047.1:c.3367C=	XP_016882536.1:p.Leu1123=
NM_181882.3:c.3469C= MANE Select	NP_870998.2:p.Leu1157=