Canonical Allele Identifier: CA1918330315

Gene: PALD1 PRF1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70598894G= , CM000672.2:g.70598894G=	GRCh38
NC_000010.10:g.72358650G= , CM000672.1:g.72358650G=	GRCh37
NC_000010.9:g.72028656G=	NCBI36
NG_009615.1:g.8882C= , LRG_94:g.8882C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697571.1:c.2425G= (PALD1)	ENSP00000513342.1:p.Ala809=
ENST00000697572.1:c.2250+34375G= (PALD1)	ENSP00000513343.1:n.2250+34375G=
ENST00000697573.1:c.2269G= (PALD1)	ENSP00000513344.1:p.Ala757=
ENST00000697577.1:n.2729G= (PALD1)
ENST00000697578.1:n.2573G= (PALD1)
ENST00000441259.2:c.827C= (PRF1) MANE Select	ENSP00000398568.1:p.Ala276=
ENST00000638674.1:c.540-1053C= (PRF1)	ENSP00000492048.1:n.540-1053C=
ENST00000639390.1:n.98-1053C= (PRF1)
ENST00000373209.2:c.827C= (PRF1)	ENSP00000362305.1:p.Ala276=
ENST00000441259.1:c.827C= (PRF1)	ENSP00000398568.1:p.Ala276=
NM_001083116.1:c.827C= , LRG_94t1:c.827C= (PRF1)	NP_001076585.1:p.Ala276=
NM_005041.4:c.827C= (PRF1)	NP_005032.2:p.Ala276=
NM_001083116.2:c.827C= (PRF1)	NP_001076585.1:p.Ala276=
NM_005041.5:c.827C= (PRF1)	NP_005032.2:p.Ala276=
NM_001083116.3:c.827C= (PRF1) MANE Select	NP_001076585.1:p.Ala276=
NM_005041.6:c.827C= (PRF1)	NP_005032.2:p.Ala276=