Canonical Allele Identifier: CA209366122

Gene: PALD1 PRF1

Linked Data

• dbSNP Id: rs532610868
• gnomAD v3: 10-70598016-A-T
• gnomAD v4: 10-70598016-A-T
• MyVariant Identifiers: chr10:g.72357772A>T (hg19) ; chr10:g.70598016A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70598016A>T , CM000672.2:g.70598016A>T	GRCh38
NC_000010.10:g.72357772A>T , CM000672.1:g.72357772A>T	GRCh37
NC_000010.9:g.72027778A>T	NCBI36
NG_009615.1:g.9760T>A , LRG_94:g.9760T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697571.1:c.2419-872A>T (PALD1)	ENSP00000513342.1:n.2419-872A>T
ENST00000697572.1:c.2250+33497A>T (PALD1)	ENSP00000513343.1:n.2250+33497A>T
ENST00000697573.1:c.2263-872A>T (PALD1)	ENSP00000513344.1:n.2263-872A>T
ENST00000697577.1:n.2723-872A>T (PALD1)
ENST00000697578.1:n.2567-872A>T (PALD1)
ENST00000441259.2:c.*37T>A (PRF1) MANE Select	ENSP00000398568.1:n.*37T>A
ENST00000638674.1:c.540-175T>A (PRF1)	ENSP00000492048.1:n.540-175T>A
ENST00000639390.1:n.98-175T>A (PRF1)
ENST00000373209.2:c.*37T>A (PRF1)	ENSP00000362305.1:n.*37T>A
ENST00000441259.1:c.*37T>A (PRF1)	ENSP00000398568.1:n.*37T>A
NM_001083116.1:c.*37T>A , LRG_94t1:c.*37T>A (PRF1)	NP_001076585.1:n.*37T>A
NM_005041.4:c.*37T>A (PRF1)	NP_005032.2:n.*37T>A
NM_001083116.2:c.*37T>A (PRF1)	NP_001076585.1:n.*37T>A
NM_005041.5:c.*37T>A (PRF1)	NP_005032.2:n.*37T>A
NM_001083116.3:c.*37T>A (PRF1) MANE Select	NP_001076585.1:n.*37T>A
NM_005041.6:c.*37T>A (PRF1)	NP_005032.2:n.*37T>A