Canonical Allele Identifier: CA1918329213

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70598375C= , CM000672.2:g.70598375C= GRCh38
NC_000010.10:g.72358131C= , CM000672.1:g.72358131C= GRCh37
NC_000010.9:g.72028137C= NCBI36
NG_009615.1:g.9401G= , LRG_94:g.9401G=

Transcript Alleles

HGVS Amino-acid change
ENST00000697571.1:c.2419-513C= (PALD1) ENSP00000513342.1:n.2419-513C=
ENST00000697572.1:c.2250+33856C= (PALD1) ENSP00000513343.1:n.2250+33856C=
ENST00000697573.1:c.2263-513C= (PALD1) ENSP00000513344.1:n.2263-513C=
ENST00000697577.1:n.2723-513C= (PALD1)
ENST00000697578.1:n.2567-513C= (PALD1)
ENST00000441259.2:c.1346G= (PRF1) MANE Select ENSP00000398568.1:p.Arg449=
ENST00000638674.1:c.540-534G= (PRF1) ENSP00000492048.1:n.540-534G=
ENST00000639390.1:n.98-534G= (PRF1)
ENST00000373209.2:c.1346G= (PRF1) ENSP00000362305.1:p.Arg449=
ENST00000441259.1:c.1346G= (PRF1) ENSP00000398568.1:p.Arg449=
NM_001083116.1:c.1346G= , LRG_94t1:c.1346G= (PRF1) NP_001076585.1:p.Arg449=
NM_005041.4:c.1346G= (PRF1) NP_005032.2:p.Arg449=
NM_001083116.2:c.1346G= (PRF1) NP_001076585.1:p.Arg449=
NM_005041.5:c.1346G= (PRF1) NP_005032.2:p.Arg449=
NM_001083116.3:c.1346G= (PRF1) MANE Select NP_001076585.1:p.Arg449=
NM_005041.6:c.1346G= (PRF1) NP_005032.2:p.Arg449=