Canonical Allele Identifier: CA1918328628

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70598029T= , CM000672.2:g.70598029T= GRCh38
NC_000010.10:g.72357785T= , CM000672.1:g.72357785T= GRCh37
NC_000010.9:g.72027791T= NCBI36
NG_009615.1:g.9747A= , LRG_94:g.9747A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697571.1:c.2419-859T= (PALD1) ENSP00000513342.1:n.2419-859T=
ENST00000697572.1:c.2250+33510T= (PALD1) ENSP00000513343.1:n.2250+33510T=
ENST00000697573.1:c.2263-859T= (PALD1) ENSP00000513344.1:n.2263-859T=
ENST00000697577.1:n.2723-859T= (PALD1)
ENST00000697578.1:n.2567-859T= (PALD1)
ENST00000441259.2:c.*24A= (PRF1) MANE Select ENSP00000398568.1:n.*24A=
ENST00000638674.1:c.540-188A= (PRF1) ENSP00000492048.1:n.540-188A=
ENST00000639390.1:n.98-188A= (PRF1)
ENST00000373209.2:c.*24A= (PRF1) ENSP00000362305.1:n.*24A=
ENST00000441259.1:c.*24A= (PRF1) ENSP00000398568.1:n.*24A=
NM_001083116.1:c.*24A= , LRG_94t1:c.*24A= (PRF1) NP_001076585.1:n.*24A=
NM_005041.4:c.*24A= (PRF1) NP_005032.2:n.*24A=
NM_001083116.2:c.*24A= (PRF1) NP_001076585.1:n.*24A=
NM_005041.5:c.*24A= (PRF1) NP_005032.2:n.*24A=
NM_001083116.3:c.*24A= (PRF1) MANE Select NP_001076585.1:n.*24A=
NM_005041.6:c.*24A= (PRF1) NP_005032.2:n.*24A=