Canonical Allele Identifier: CA2335960962
Gene: PRX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40395018_40395026delinsCCCTCCCTT , CM000681.2:g.40395018_40395026delinsCCCTCCCTT GRCh38
NC_000019.9:g.40900925_40900933delinsCCCTCCCTT , CM000681.1:g.40900925_40900933delinsCCCTCCCTT GRCh37
NC_000019.8:g.45592765_45592773delinsCCCTCCCTT NCBI36
NG_007979.1:g.23339_23347delinsAAGGGAGGG , LRG_265:g.23339_23347delinsAAGGGAGGG
NG_051224.1:g.196_204delinsAAGGGAGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000324001.8:c.3326_3334delinsAAGGGAGGG MANE Select ENSP00000326018.6:p.Glu1109=
ENST00000673881.1:c.2909_2917delinsAAGGGAGGG ENSP00000501070.1:p.Glu970=
ENST00000674005.2:c.3611_3619delinsAAGGGAGGG ENSP00000501261.1:p.Glu1204=
ENST00000674773.1:c.2909_2917delinsAAGGGAGGG ENSP00000502579.1:p.Glu970=
ENST00000675517.1:c.3201_3209delinsAAGGGAGGG
ENST00000676076.1:c.3187_3195delinsAAGGGAGGG
ENST00000676260.1:c.3288_3296delinsAAGGGAGGG
ENST00000676316.1:c.3213_3221delinsAAGGGAGGG
ENST00000291825.11:c.*3531_*3539delinsAAGGGAGGG ENSP00000291825.6:n.*3531_*3539delinsAAGGGAGGG
ENST00000324001.7:c.3326_3334delinsAAGGGAGGG ENSP00000326018.6:p.Glu1109=
NM_020956.2:c.*3531_*3539delinsAAGGGAGGG , LRG_265t1:c.*3531_*3539delinsAAGGGAGGG NP_066007.1:n.*3531_*3539delinsAAGGGAGGG
NM_181882.2:c.3326_3334delinsAAGGGAGGG , LRG_265t2:c.3326_3334delinsAAGGGAGGG NP_870998.2:p.Glu1109=
XM_011527171.1:c.3326_3334delinsAAGGGAGGG XP_011525473.1:p.Glu1109=
XM_011527171.2:c.3326_3334delinsAAGGGAGGG XP_011525473.1:p.Glu1109=
XM_017027046.1:c.3224_3232delinsAAGGGAGGG XP_016882535.1:p.Glu1075=
XM_017027047.1:c.3224_3232delinsAAGGGAGGG XP_016882536.1:p.Glu1075=
NM_181882.3:c.3326_3334delinsAAGGGAGGG MANE Select NP_870998.2:p.Glu1109=