Canonical Allele Identifier: CA308419571

Gene: PRX

Linked Data

• dbSNP Id: rs35735227
• MyVariant Identifiers: chr19:g.40902029_40902030insG (hg19) ; chr19:g.40396122_40396123insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396126dup , CM000681.2:g.40396126dup	GRCh38
NC_000019.9:g.40902033dup , CM000681.1:g.40902033dup	GRCh37
NC_000019.8:g.45593873dup	NCBI36
NG_007979.1:g.22242dup , LRG_265:g.22242dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000324001.8:c.2229dup MANE Select	ENSP00000326018.6:p.Glu744ArgfsTer?
ENST00000673881.1:c.1812dup	ENSP00000501070.1:p.Glu605ArgfsTer?
ENST00000674005.2:c.2514dup	ENSP00000501261.1:p.Glu839ArgfsTer?
ENST00000674773.1:c.1812dup	ENSP00000502579.1:p.Glu605ArgfsTer?
ENST00000675517.1:c.2104dup
ENST00000676076.1:c.2090dup
ENST00000676260.1:c.2191dup
ENST00000676316.1:c.2116dup
ENST00000291825.11:c.*2434dup	ENSP00000291825.6:n.*2434dup
ENST00000324001.7:c.2229dup	ENSP00000326018.6:p.Glu744ArgfsTer?
NM_020956.2:c.*2434dup , LRG_265t1:c.*2434dup	NP_066007.1:n.*2434dup
NM_181882.2:c.2229dup , LRG_265t2:c.2229dup	NP_870998.2:p.Glu744ArgfsTer?
XM_011527171.1:c.2229dup	XP_011525473.1:p.Glu744ArgfsTer?
XM_011527171.2:c.2229dup	XP_011525473.1:p.Glu744ArgfsTer?
XM_017027046.1:c.2127dup	XP_016882535.1:p.Glu710ArgfsTer?
XM_017027047.1:c.2127dup	XP_016882536.1:p.Glu710ArgfsTer?
NM_181882.3:c.2229dup MANE Select	NP_870998.2:p.Glu744ArgfsTer?