Canonical Allele Identifier: CA2335961531
Gene: PRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40396231_40396309delinsTGGGAGGTGCACATCGGGCACGGCCATTTCAGGCACCTTGGGGAGTTTCATCTCTGAGACTTTTGGCAGCTGCACCTCG , CM000681.2:g.40396231_40396309delinsTGGGAGGTGCACATCGGGCACGGCCATTTCAGGCACCTTGGGGAGTTTCATCTCTGAGACTTTTGGCAGCTGCACCTCG GRCh38
NC_000019.9:g.40902138_40902216delinsTGGGAGGTGCACATCGGGCACGGCCATTTCAGGCACCTTGGGGAGTTTCATCTCTGAGACTTTTGGCAGCTGCACCTCG , CM000681.1:g.40902138_40902216delinsTGGGAGGTGCACATCGGGCACGGCCATTTCAGGCACCTTGGGGAGTTTCATCTCTGAGACTTTTGGCAGCTGCACCTCG GRCh37
NC_000019.8:g.45593978_45594056delinsTGGGAGGTGCACATCGGGCACGGCCATTTCAGGCACCTTGGGGAGTTTCATCTCTGAGACTTTTGGCAGCTGCACCTCG NCBI36
NG_007979.1:g.22056_22134delinsCGAGGTGCAGCTGCCAAAAGTCTCAGAGATGAAACTCCCCAAGGTGCCTGAAATGGCCGTGCCCGATGTGCACCTCCCA , LRG_265:g.22056_22134delinsCGAGGTGCAGCTGCCAAAAGTCTCAGAGATGAAACTCCCCAAGGTGCCTGAAATGGCCGTGCCCGATGTGCACCTCCCA

Transcript Alleles

HGVS Amino-acid change
ENST00000324001.8:c.2043_2121delinsCGAGGTGCAGCTGCCAAAAGTCTCAGAGATGAAACTCCCCAAGGTGCCTGAAATGGCCGTGCCCGATGTGCACCTCCCA MANE Select ENSP00000326018.6:p.Pro681=
ENST00000673881.1:c.1626_1704delinsCGAGGTGCAGCTGCCAAAAGTCTCAGAGATGAAACTCCCCAAGGTGCCTGAAATGGCCGTGCCCGATGTGCACCTCCCA ENSP00000501070.1:p.Pro542=
ENST00000674005.2:c.2328_2406delinsCGAGGTGCAGCTGCCAAAAGTCTCAGAGATGAAACTCCCCAAGGTGCCTGAAATGGCCGTGCCCGATGTGCACCTCCCA ENSP00000501261.1:p.Pro776=
ENST00000674773.1:c.1626_1704delinsCGAGGTGCAGCTGCCAAAAGTCTCAGAGATGAAACTCCCCAAGGTGCCTGAAATGGCCGTGCCCGATGTGCACCTCCCA ENSP00000502579.1:p.Pro542=
ENST00000675517.1:c.1918_1996delinsCGAGGTGCAGCTGCCAAAAGTCTCAGAGATGAAACTCCCCAAGGTGCCTGAAATGGCCGTGCCCGATGTGCACCTCCCA
ENST00000676076.1:c.1904_1982delinsCGAGGTGCAGCTGCCAAAAGTCTCAGAGATGAAACTCCCCAAGGTGCCTGAAATGGCCGTGCCCGATGTGCACCTCCCA
ENST00000676260.1:c.2005_2083delinsCGAGGTGCAGCTGCCAAAAGTCTCAGAGATGAAACTCCCCAAGGTGCCTGAAATGGCCGTGCCCGATGTGCACCTCCCA
ENST00000676316.1:c.1930_2008delinsCGAGGTGCAGCTGCCAAAAGTCTCAGAGATGAAACTCCCCAAGGTGCCTGAAATGGCCGTGCCCGATGTGCACCTCCCA
ENST00000291825.11:c.*2248_*2326delinsCGAGGTGCAGCTGCCAAAAGTCTCAGAGATGAAACTCCCCAAGGTGCCTGAAATGGCCGTGCCCGATGTGCACCTCCCA ENSP00000291825.6:n.*2248_*2326delinsCGAG...
ENST00000324001.7:c.2043_2121delinsCGAGGTGCAGCTGCCAAAAGTCTCAGAGATGAAACTCCCCAAGGTGCCTGAAATGGCCGTGCCCGATGTGCACCTCCCA ENSP00000326018.6:p.Pro681=
NM_020956.2:c.*2248_*2326delinsCGAGGTGCAGCTGCCAAAAGTCTCAGAGATGAAACTCCCCAAGGTGCCTGAAATGGCCGTGCCCGATGTGCACCTCCCA , LRG_265t1:c.*2248_*2326delinsCGAGGTGCAGCTGCCAAAAGTCTCAGAGATGAAACTCCCCAAGGTGCCTGAAATGGCCGTGCCCGATGTGCACCTCCCA NP_066007.1:n.*2248_*2326delinsCGAGGTGCAG...
NM_181882.2:c.2043_2121delinsCGAGGTGCAGCTGCCAAAAGTCTCAGAGATGAAACTCCCCAAGGTGCCTGAAATGGCCGTGCCCGATGTGCACCTCCCA , LRG_265t2:c.2043_2121delinsCGAGGTGCAGCTGCCAAAAGTCTCAGAGATGAAACTCCCCAAGGTGCCTGAAATGGCCGTGCCCGATGTGCACCTCCCA NP_870998.2:p.Pro681=
XM_011527171.1:c.2043_2121delinsCGAGGTGCAGCTGCCAAAAGTCTCAGAGATGAAACTCCCCAAGGTGCCTGAAATGGCCGTGCCCGATGTGCACCTCCCA XP_011525473.1:p.Pro681=
XM_011527171.2:c.2043_2121delinsCGAGGTGCAGCTGCCAAAAGTCTCAGAGATGAAACTCCCCAAGGTGCCTGAAATGGCCGTGCCCGATGTGCACCTCCCA XP_011525473.1:p.Pro681=
XM_017027046.1:c.1941_2019delinsCGAGGTGCAGCTGCCAAAAGTCTCAGAGATGAAACTCCCCAAGGTGCCTGAAATGGCCGTGCCCGATGTGCACCTCCCA XP_016882535.1:p.Pro647=
XM_017027047.1:c.1941_2019delinsCGAGGTGCAGCTGCCAAAAGTCTCAGAGATGAAACTCCCCAAGGTGCCTGAAATGGCCGTGCCCGATGTGCACCTCCCA XP_016882536.1:p.Pro647=
NM_181882.3:c.2043_2121delinsCGAGGTGCAGCTGCCAAAAGTCTCAGAGATGAAACTCCCCAAGGTGCCTGAAATGGCCGTGCCCGATGTGCACCTCCCA MANE Select NP_870998.2:p.Pro681=