Canonical Allele Identifier: CA1918330441

Gene: PALD1 PRF1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70598965G= , CM000672.2:g.70598965G=	GRCh38
NC_000010.10:g.72358721G= , CM000672.1:g.72358721G=	GRCh37
NC_000010.9:g.72028727G=	NCBI36
NG_009615.1:g.8811C= , LRG_94:g.8811C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697571.1:c.2496G= (PALD1)	ENSP00000513342.1:p.Ser832=
ENST00000697572.1:c.2250+34446G= (PALD1)	ENSP00000513343.1:n.2250+34446G=
ENST00000697573.1:c.2340G= (PALD1)	ENSP00000513344.1:p.Ser780=
ENST00000697577.1:n.2800G= (PALD1)
ENST00000697578.1:n.2644G= (PALD1)
ENST00000441259.2:c.756C= (PRF1) MANE Select	ENSP00000398568.1:p.Asn252=
ENST00000638674.1:c.540-1124C= (PRF1)	ENSP00000492048.1:n.540-1124C=
ENST00000639390.1:n.98-1124C= (PRF1)
ENST00000373209.2:c.756C= (PRF1)	ENSP00000362305.1:p.Asn252=
ENST00000441259.1:c.756C= (PRF1)	ENSP00000398568.1:p.Asn252=
NM_001083116.1:c.756C= , LRG_94t1:c.756C= (PRF1)	NP_001076585.1:p.Asn252=
NM_005041.4:c.756C= (PRF1)	NP_005032.2:p.Asn252=
NM_001083116.2:c.756C= (PRF1)	NP_001076585.1:p.Asn252=
NM_005041.5:c.756C= (PRF1)	NP_005032.2:p.Asn252=
NM_001083116.3:c.756C= (PRF1) MANE Select	NP_001076585.1:p.Asn252=
NM_005041.6:c.756C= (PRF1)	NP_005032.2:p.Asn252=