Canonical Allele Identifier: CA1918322860

Gene: PALD1 PRF1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70600818_70600819delinsAG , CM000672.2:g.70600818_70600819delinsAG	GRCh38
NC_000010.10:g.72360574_72360575delinsAG , CM000672.1:g.72360574_72360575delinsAG	GRCh37
NC_000010.9:g.72030580_72030581delinsAG	NCBI36
NG_009615.1:g.6957_6958delinsCT , LRG_94:g.6957_6958delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697571.1:c.*17+1734_*17+1735delinsAG (PALD1)	ENSP00000513342.1:n.*17+1734_*17+1735delinsAG
ENST00000697572.1:c.2250+36299_2250+36300delinsAG (PALD1)	ENSP00000513343.1:n.2250+36299_2250+36300delinsAG
ENST00000697573.1:c.*17+1734_*17+1735delinsAG (PALD1)	ENSP00000513344.1:n.*17+1734_*17+1735delinsAG
ENST00000697577.1:n.2919+1734_2919+1735delinsAG (PALD1)
ENST00000697578.1:n.2763+1734_2763+1735delinsAG (PALD1)
ENST00000441259.2:c.84_85delinsCT (PRF1) MANE Select	ENSP00000398568.1:p.Arg28=
ENST00000638674.1:c.84_85delinsCT (PRF1)	ENSP00000492048.1:p.Arg28=
ENST00000639390.1:n.97+1826_97+1827delinsCT (PRF1)
ENST00000373209.2:c.84_85delinsCT (PRF1)	ENSP00000362305.1:p.Arg28=
ENST00000441259.1:c.84_85delinsCT (PRF1)	ENSP00000398568.1:p.Arg28=
NM_001083116.1:c.84_85delinsCT , LRG_94t1:c.84_85delinsCT (PRF1)	NP_001076585.1:p.Arg28=
NM_005041.4:c.84_85delinsCT (PRF1)	NP_005032.2:p.Arg28=
NM_001083116.2:c.84_85delinsCT (PRF1)	NP_001076585.1:p.Arg28=
NM_005041.5:c.84_85delinsCT (PRF1)	NP_005032.2:p.Arg28=
NM_001083116.3:c.84_85delinsCT (PRF1) MANE Select	NP_001076585.1:p.Arg28=
NM_005041.6:c.84_85delinsCT (PRF1)	NP_005032.2:p.Arg28=