Canonical Allele Identifier: CA405893856

Gene: PRX

Linked Data

• MyVariant Identifiers: chr19:g.40900852G>A (hg19) ; chr19:g.40394945G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394945G>A , CM000681.2:g.40394945G>A	GRCh38
NC_000019.9:g.40900852G>A , CM000681.1:g.40900852G>A	GRCh37
NC_000019.8:g.45592692G>A	NCBI36
NG_007979.1:g.23420C>T , LRG_265:g.23420C>T
NG_051224.1:g.277C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.3407C>T MANE Select	ENSP00000326018.6:p.Thr1136Ile
ENST00000673881.1:c.2990C>T	ENSP00000501070.1:p.Thr997Ile
ENST00000674005.2:c.3692C>T	ENSP00000501261.1:p.Thr1231Ile
ENST00000674773.1:c.2990C>T	ENSP00000502579.1:p.Thr997Ile
ENST00000675517.1:c.3282C>T
ENST00000676076.1:c.3268C>T
ENST00000676260.1:c.3369C>T
ENST00000676316.1:c.3294C>T
ENST00000291825.11:c.*3612C>T	ENSP00000291825.6:n.*3612C>T
ENST00000324001.7:c.3407C>T	ENSP00000326018.6:p.Thr1136Ile
NM_020956.2:c.*3612C>T , LRG_265t1:c.*3612C>T	NP_066007.1:n.*3612C>T
NM_181882.2:c.3407C>T , LRG_265t2:c.3407C>T	NP_870998.2:p.Thr1136Ile
XM_011527171.1:c.3407C>T	XP_011525473.1:p.Thr1136Ile
XM_011527171.2:c.3407C>T	XP_011525473.1:p.Thr1136Ile
XM_017027046.1:c.3305C>T	XP_016882535.1:p.Thr1102Ile
XM_017027047.1:c.3305C>T	XP_016882536.1:p.Thr1102Ile
NM_181882.3:c.3407C>T MANE Select	NP_870998.2:p.Thr1136Ile