Canonical Allele Identifier: CA1918328675

Gene: PALD1 PRF1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70598062G= , CM000672.2:g.70598062G=	GRCh38
NC_000010.10:g.72357818G= , CM000672.1:g.72357818G=	GRCh37
NC_000010.9:g.72027824G=	NCBI36
NG_009615.1:g.9714C= , LRG_94:g.9714C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697571.1:c.2419-826G= (PALD1)	ENSP00000513342.1:n.2419-826G=
ENST00000697572.1:c.2250+33543G= (PALD1)	ENSP00000513343.1:n.2250+33543G=
ENST00000697573.1:c.2263-826G= (PALD1)	ENSP00000513344.1:n.2263-826G=
ENST00000697577.1:n.2723-826G= (PALD1)
ENST00000697578.1:n.2567-826G= (PALD1)
ENST00000441259.2:c.1659C= (PRF1) MANE Select	ENSP00000398568.1:p.Ala553=
ENST00000638674.1:c.540-221C= (PRF1)	ENSP00000492048.1:n.540-221C=
ENST00000639390.1:n.98-221C= (PRF1)
ENST00000373209.2:c.1659C= (PRF1)	ENSP00000362305.1:p.Ala553=
ENST00000441259.1:c.1659C= (PRF1)	ENSP00000398568.1:p.Ala553=
NM_001083116.1:c.1659C= , LRG_94t1:c.1659C= (PRF1)	NP_001076585.1:p.Ala553=
NM_005041.4:c.1659C= (PRF1)	NP_005032.2:p.Ala553=
NM_001083116.2:c.1659C= (PRF1)	NP_001076585.1:p.Ala553=
NM_005041.5:c.1659C= (PRF1)	NP_005032.2:p.Ala553=
NM_001083116.3:c.1659C= (PRF1) MANE Select	NP_001076585.1:p.Ala553=
NM_005041.6:c.1659C= (PRF1)	NP_005032.2:p.Ala553=