Canonical Allele Identifier: CA376958442

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70598927T>A , CM000672.2:g.70598927T>A GRCh38
NC_000010.10:g.72358683T>A , CM000672.1:g.72358683T>A GRCh37
NC_000010.9:g.72028689T>A NCBI36
NG_009615.1:g.8849A>T , LRG_94:g.8849A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000697571.1:c.2458T>A (PALD1) ENSP00000513342.1:p.Leu820Met
ENST00000697572.1:c.2250+34408T>A (PALD1) ENSP00000513343.1:n.2250+34408T>A
ENST00000697573.1:c.2302T>A (PALD1) ENSP00000513344.1:p.Leu768Met
ENST00000697577.1:n.2762T>A (PALD1)
ENST00000697578.1:n.2606T>A (PALD1)
ENST00000441259.2:c.794A>T (PRF1) MANE Select ENSP00000398568.1:p.Asn265Ile
ENST00000638674.1:c.540-1086A>T (PRF1) ENSP00000492048.1:n.540-1086A>T
ENST00000639390.1:n.98-1086A>T (PRF1)
ENST00000373209.2:c.794A>T (PRF1) ENSP00000362305.1:p.Asn265Ile
ENST00000441259.1:c.794A>T (PRF1) ENSP00000398568.1:p.Asn265Ile
NM_001083116.1:c.794A>T , LRG_94t1:c.794A>T (PRF1) NP_001076585.1:p.Asn265Ile
NM_005041.4:c.794A>T (PRF1) NP_005032.2:p.Asn265Ile
NM_001083116.2:c.794A>T (PRF1) NP_001076585.1:p.Asn265Ile
NM_005041.5:c.794A>T (PRF1) NP_005032.2:p.Asn265Ile
NM_001083116.3:c.794A>T (PRF1) MANE Select NP_001076585.1:p.Asn265Ile
NM_005041.6:c.794A>T (PRF1) NP_005032.2:p.Asn265Ile