Canonical Allele Identifier: CA5538898

Gene: PALD1 PRF1

Linked Data

• ClinVar Variation Id: 1122932
• ClinVar RCV Id: RCV001453771
• dbSNP Id: rs745670464
• ExAC: 10:72358610 C / T
• gnomAD v2: 10-72358610-C-T
• gnomAD v3: 10-70598854-C-T
• gnomAD v4: 10-70598854-C-T
• MyVariant Identifiers: chr10:g.72358610C>T (hg19) ; chr10:g.70598854C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70598854C>T , CM000672.2:g.70598854C>T	GRCh38
NC_000010.10:g.72358610C>T , CM000672.1:g.72358610C>T	GRCh37
NC_000010.9:g.72028616C>T	NCBI36
NG_009615.1:g.8922G>A , LRG_94:g.8922G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697571.1:c.2419-34C>T (PALD1)	ENSP00000513342.1:n.2419-34C>T
ENST00000697572.1:c.2250+34335C>T (PALD1)	ENSP00000513343.1:n.2250+34335C>T
ENST00000697573.1:c.2263-34C>T (PALD1)	ENSP00000513344.1:n.2263-34C>T
ENST00000697577.1:n.2723-34C>T (PALD1)
ENST00000697578.1:n.2567-34C>T (PALD1)
ENST00000441259.2:c.867G>A (PRF1) MANE Select	ENSP00000398568.1:p.Thr289=
ENST00000638674.1:c.540-1013G>A (PRF1)	ENSP00000492048.1:n.540-1013G>A
ENST00000639390.1:n.98-1013G>A (PRF1)
ENST00000373209.2:c.867G>A (PRF1)	ENSP00000362305.1:p.Thr289=
ENST00000441259.1:c.867G>A (PRF1)	ENSP00000398568.1:p.Thr289=
NM_001083116.1:c.867G>A , LRG_94t1:c.867G>A (PRF1)	NP_001076585.1:p.Thr289=
NM_005041.4:c.867G>A (PRF1)	NP_005032.2:p.Thr289=
NM_001083116.2:c.867G>A (PRF1)	NP_001076585.1:p.Thr289=
NM_005041.5:c.867G>A (PRF1)	NP_005032.2:p.Thr289=
NM_001083116.3:c.867G>A (PRF1) MANE Select	NP_001076585.1:p.Thr289=
NM_005041.6:c.867G>A (PRF1)	NP_005032.2:p.Thr289=