Canonical Allele Identifier: CA1918329559

Gene: PALD1 PRF1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70598553G= , CM000672.2:g.70598553G=	GRCh38
NC_000010.10:g.72358309G= , CM000672.1:g.72358309G=	GRCh37
NC_000010.9:g.72028315G=	NCBI36
NG_009615.1:g.9223C= , LRG_94:g.9223C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697571.1:c.2419-335G= (PALD1)	ENSP00000513342.1:n.2419-335G=
ENST00000697572.1:c.2250+34034G= (PALD1)	ENSP00000513343.1:n.2250+34034G=
ENST00000697573.1:c.2263-335G= (PALD1)	ENSP00000513344.1:n.2263-335G=
ENST00000697577.1:n.2723-335G= (PALD1)
ENST00000697578.1:n.2567-335G= (PALD1)
ENST00000441259.2:c.1168C= (PRF1) MANE Select	ENSP00000398568.1:p.Arg390=
ENST00000638674.1:c.540-712C= (PRF1)	ENSP00000492048.1:n.540-712C=
ENST00000639390.1:n.98-712C= (PRF1)
ENST00000373209.2:c.1168C= (PRF1)	ENSP00000362305.1:p.Arg390=
ENST00000441259.1:c.1168C= (PRF1)	ENSP00000398568.1:p.Arg390=
NM_001083116.1:c.1168C= , LRG_94t1:c.1168C= (PRF1)	NP_001076585.1:p.Arg390=
NM_005041.4:c.1168C= (PRF1)	NP_005032.2:p.Arg390=
NM_001083116.2:c.1168C= (PRF1)	NP_001076585.1:p.Arg390=
NM_005041.5:c.1168C= (PRF1)	NP_005032.2:p.Arg390=
NM_001083116.3:c.1168C= (PRF1) MANE Select	NP_001076585.1:p.Arg390=
NM_005041.6:c.1168C= (PRF1)	NP_005032.2:p.Arg390=