Canonical Allele Identifier: CA2736045053

Gene: PRX

Linked Data

• dbSNP Id: rs2145729027

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396179_40396195del , CM000681.2:g.40396179_40396195del	GRCh38
NC_000019.9:g.40902086_40902102del , CM000681.1:g.40902086_40902102del	GRCh37
NC_000019.8:g.45593926_45593942del	NCBI36
NG_007979.1:g.22171_22187del , LRG_265:g.22171_22187del

Transcript Alleles

HGVS	Amino-acid change
ENST00000324001.8:c.2158_2174del MANE Select	ENSP00000326018.6:p.Pro720ArgfsTer9
ENST00000673881.1:c.1741_1757del	ENSP00000501070.1:p.Pro581ArgfsTer9
ENST00000674005.2:c.2443_2459del	ENSP00000501261.1:p.Pro815ArgfsTer9
ENST00000674773.1:c.1741_1757del	ENSP00000502579.1:p.Pro581ArgfsTer9
ENST00000675517.1:c.2033_2049del
ENST00000676076.1:c.2019_2035del
ENST00000676260.1:c.2120_2136del
ENST00000676316.1:c.2045_2061del
ENST00000291825.11:c.*2363_*2379del	ENSP00000291825.6:n.*2363_*2379del
ENST00000324001.7:c.2158_2174del	ENSP00000326018.6:p.Pro720ArgfsTer9
NM_020956.2:c.*2363_*2379del , LRG_265t1:c.*2363_*2379del	NP_066007.1:n.*2363_*2379del
NM_181882.2:c.2158_2174del , LRG_265t2:c.2158_2174del	NP_870998.2:p.Pro720ArgfsTer9
XM_011527171.1:c.2158_2174del	XP_011525473.1:p.Pro720ArgfsTer9
XM_011527171.2:c.2158_2174del	XP_011525473.1:p.Pro720ArgfsTer9
XM_017027046.1:c.2056_2072del	XP_016882535.1:p.Pro686ArgfsTer9
XM_017027047.1:c.2056_2072del	XP_016882536.1:p.Pro686ArgfsTer9
NM_181882.3:c.2158_2174del MANE Select	NP_870998.2:p.Pro720ArgfsTer9