Canonical Allele Identifier: CA507678561

Gene: PRX

Linked Data

• MyVariant Identifiers: chr19:g.40900869T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394962T>A , CM000681.2:g.40394962T>A	GRCh38
NC_000019.9:g.40900869T>A , CM000681.1:g.40900869T>A	GRCh37
NC_000019.8:g.45592709T>A	NCBI36
NG_007979.1:g.23403A>T , LRG_265:g.23403A>T
NG_051224.1:g.260A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.3390A>T MANE Select	ENSP00000326018.6:p.Thr1130=
ENST00000673881.1:c.2973A>T	ENSP00000501070.1:p.Thr991=
ENST00000674005.2:c.3675A>T	ENSP00000501261.1:p.Thr1225=
ENST00000674773.1:c.2973A>T	ENSP00000502579.1:p.Thr991=
ENST00000675517.1:c.3265A>T
ENST00000676076.1:c.3251A>T
ENST00000676260.1:c.3352A>T
ENST00000676316.1:c.3277A>T
ENST00000291825.11:c.*3595A>T	ENSP00000291825.6:n.*3595A>T
ENST00000324001.7:c.3390A>T	ENSP00000326018.6:p.Thr1130=
NM_020956.2:c.*3595A>T , LRG_265t1:c.*3595A>T	NP_066007.1:n.*3595A>T
NM_181882.2:c.3390A>T , LRG_265t2:c.3390A>T	NP_870998.2:p.Thr1130=
XM_011527171.1:c.3390A>T	XP_011525473.1:p.Thr1130=
XM_011527171.2:c.3390A>T	XP_011525473.1:p.Thr1130=
XM_017027046.1:c.3288A>T	XP_016882535.1:p.Thr1096=
XM_017027047.1:c.3288A>T	XP_016882536.1:p.Thr1096=
NM_181882.3:c.3390A>T MANE Select	NP_870998.2:p.Thr1130=