Canonical Allele Identifier: CA5538822

Gene: PALD1 PRF1

Linked Data

• ClinVar Variation Id: 1523906
• ClinVar RCV Id: RCV002031318
• dbSNP Id: rs374588624
• ExAC: 10:72358360 G / A
• gnomAD v2: 10-72358360-G-A
• gnomAD v3: 10-70598604-G-A
• gnomAD v4: 10-70598604-G-A
• MyVariant Identifiers: chr10:g.72358360G>A (hg19) ; chr10:g.70598604G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70598604G>A , CM000672.2:g.70598604G>A	GRCh38
NC_000010.10:g.72358360G>A , CM000672.1:g.72358360G>A	GRCh37
NC_000010.9:g.72028366G>A	NCBI36
NG_009615.1:g.9172C>T , LRG_94:g.9172C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697571.1:c.2419-284G>A (PALD1)	ENSP00000513342.1:n.2419-284G>A
ENST00000697572.1:c.2250+34085G>A (PALD1)	ENSP00000513343.1:n.2250+34085G>A
ENST00000697573.1:c.2263-284G>A (PALD1)	ENSP00000513344.1:n.2263-284G>A
ENST00000697577.1:n.2723-284G>A (PALD1)
ENST00000697578.1:n.2567-284G>A (PALD1)
ENST00000441259.2:c.1117C>T (PRF1) MANE Select	ENSP00000398568.1:p.Arg373Cys
ENST00000638674.1:c.540-763C>T (PRF1)	ENSP00000492048.1:n.540-763C>T
ENST00000639390.1:n.98-763C>T (PRF1)
ENST00000373209.2:c.1117C>T (PRF1)	ENSP00000362305.1:p.Arg373Cys
ENST00000441259.1:c.1117C>T (PRF1)	ENSP00000398568.1:p.Arg373Cys
NM_001083116.1:c.1117C>T , LRG_94t1:c.1117C>T (PRF1)	NP_001076585.1:p.Arg373Cys
NM_005041.4:c.1117C>T (PRF1)	NP_005032.2:p.Arg373Cys
NM_001083116.2:c.1117C>T (PRF1)	NP_001076585.1:p.Arg373Cys
NM_005041.5:c.1117C>T (PRF1)	NP_005032.2:p.Arg373Cys
NM_001083116.3:c.1117C>T (PRF1) MANE Select	NP_001076585.1:p.Arg373Cys
NM_005041.6:c.1117C>T (PRF1)	NP_005032.2:p.Arg373Cys