Canonical Allele Identifier: CA376960075

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70600794A>T , CM000672.2:g.70600794A>T GRCh38
NC_000010.10:g.72360550A>T , CM000672.1:g.72360550A>T GRCh37
NC_000010.9:g.72030556A>T NCBI36
NG_009615.1:g.6982T>A , LRG_94:g.6982T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000697571.1:c.*17+1710A>T (PALD1) ENSP00000513342.1:n.*17+1710A>T
ENST00000697572.1:c.2250+36275A>T (PALD1) ENSP00000513343.1:n.2250+36275A>T
ENST00000697573.1:c.*17+1710A>T (PALD1) ENSP00000513344.1:n.*17+1710A>T
ENST00000697577.1:n.2919+1710A>T (PALD1)
ENST00000697578.1:n.2763+1710A>T (PALD1)
ENST00000441259.2:c.109T>A (PRF1) MANE Select ENSP00000398568.1:p.Phe37Ile
ENST00000638674.1:c.109T>A (PRF1) ENSP00000492048.1:p.Phe37Ile
ENST00000639390.1:n.97+1851T>A (PRF1)
ENST00000373209.2:c.109T>A (PRF1) ENSP00000362305.1:p.Phe37Ile
ENST00000441259.1:c.109T>A (PRF1) ENSP00000398568.1:p.Phe37Ile
NM_001083116.1:c.109T>A , LRG_94t1:c.109T>A (PRF1) NP_001076585.1:p.Phe37Ile
NM_005041.4:c.109T>A (PRF1) NP_005032.2:p.Phe37Ile
NM_001083116.2:c.109T>A (PRF1) NP_001076585.1:p.Phe37Ile
NM_005041.5:c.109T>A (PRF1) NP_005032.2:p.Phe37Ile
NM_001083116.3:c.109T>A (PRF1) MANE Select NP_001076585.1:p.Phe37Ile
NM_005041.6:c.109T>A (PRF1) NP_005032.2:p.Phe37Ile