Canonical Allele Identifier: CA376960181

Gene: PALD1 PRF1

Linked Data

• dbSNP Id: rs1309681334
• MyVariant Identifiers: chr10:g.72360601G>T (hg19) ; chr10:g.70600845G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70600845G>T , CM000672.2:g.70600845G>T	GRCh38
NC_000010.10:g.72360601G>T , CM000672.1:g.72360601G>T	GRCh37
NC_000010.9:g.72030607G>T	NCBI36
NG_009615.1:g.6931C>A , LRG_94:g.6931C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697571.1:c.*17+1761G>T (PALD1)	ENSP00000513342.1:n.*17+1761G>T
ENST00000697572.1:c.2250+36326G>T (PALD1)	ENSP00000513343.1:n.2250+36326G>T
ENST00000697573.1:c.*17+1761G>T (PALD1)	ENSP00000513344.1:n.*17+1761G>T
ENST00000697577.1:n.2919+1761G>T (PALD1)
ENST00000697578.1:n.2763+1761G>T (PALD1)
ENST00000441259.2:c.58C>A (PRF1) MANE Select	ENSP00000398568.1:p.Pro20Thr
ENST00000638674.1:c.58C>A (PRF1)	ENSP00000492048.1:p.Pro20Thr
ENST00000639390.1:n.97+1800C>A (PRF1)
ENST00000373209.2:c.58C>A (PRF1)	ENSP00000362305.1:p.Pro20Thr
ENST00000441259.1:c.58C>A (PRF1)	ENSP00000398568.1:p.Pro20Thr
NM_001083116.1:c.58C>A , LRG_94t1:c.58C>A (PRF1)	NP_001076585.1:p.Pro20Thr
NM_005041.4:c.58C>A (PRF1)	NP_005032.2:p.Pro20Thr
NM_001083116.2:c.58C>A (PRF1)	NP_001076585.1:p.Pro20Thr
NM_005041.5:c.58C>A (PRF1)	NP_005032.2:p.Pro20Thr
NM_001083116.3:c.58C>A (PRF1) MANE Select	NP_001076585.1:p.Pro20Thr
NM_005041.6:c.58C>A (PRF1)	NP_005032.2:p.Pro20Thr