Canonical Allele Identifier: CA1918329538

Gene: PALD1 PRF1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70598545_70598546delinsTG , CM000672.2:g.70598545_70598546delinsTG	GRCh38
NC_000010.10:g.72358301_72358302delinsTG , CM000672.1:g.72358301_72358302delinsTG	GRCh37
NC_000010.9:g.72028307_72028308delinsTG	NCBI36
NG_009615.1:g.9230_9231delinsCA , LRG_94:g.9230_9231delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697571.1:c.2419-343_2419-342delinsTG (PALD1)	ENSP00000513342.1:n.2419-343_2419-342delinsTG
ENST00000697572.1:c.2250+34026_2250+34027delinsTG (PALD1)	ENSP00000513343.1:n.2250+34026_2250+34027delinsTG
ENST00000697573.1:c.2263-343_2263-342delinsTG (PALD1)	ENSP00000513344.1:n.2263-343_2263-342delinsTG
ENST00000697577.1:n.2723-343_2723-342delinsTG (PALD1)
ENST00000697578.1:n.2567-343_2567-342delinsTG (PALD1)
ENST00000441259.2:c.1175_1176delinsCA (PRF1) MANE Select	ENSP00000398568.1:p.Pro392=
ENST00000638674.1:c.540-705_540-704delinsCA (PRF1)	ENSP00000492048.1:n.540-705_540-704delinsCA
ENST00000639390.1:n.98-705_98-704delinsCA (PRF1)
ENST00000373209.2:c.1175_1176delinsCA (PRF1)	ENSP00000362305.1:p.Pro392=
ENST00000441259.1:c.1175_1176delinsCA (PRF1)	ENSP00000398568.1:p.Pro392=
NM_001083116.1:c.1175_1176delinsCA , LRG_94t1:c.1175_1176delinsCA (PRF1)	NP_001076585.1:p.Pro392=
NM_005041.4:c.1175_1176delinsCA (PRF1)	NP_005032.2:p.Pro392=
NM_001083116.2:c.1175_1176delinsCA (PRF1)	NP_001076585.1:p.Pro392=
NM_005041.5:c.1175_1176delinsCA (PRF1)	NP_005032.2:p.Pro392=
NM_001083116.3:c.1175_1176delinsCA (PRF1) MANE Select	NP_001076585.1:p.Pro392=
NM_005041.6:c.1175_1176delinsCA (PRF1)	NP_005032.2:p.Pro392=