Canonical Allele Identifier: CA2609520378

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70600907C>A , CM000672.2:g.70600907C>A GRCh38
NC_000010.10:g.72360663C>A , CM000672.1:g.72360663C>A GRCh37
NC_000010.9:g.72030669C>A NCBI36
NG_009615.1:g.6869G>T , LRG_94:g.6869G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000697571.1:c.*17+1823C>A (PALD1) ENSP00000513342.1:n.*17+1823C>A
ENST00000697572.1:c.2250+36388C>A (PALD1) ENSP00000513343.1:n.2250+36388C>A
ENST00000697573.1:c.*17+1823C>A (PALD1) ENSP00000513344.1:n.*17+1823C>A
ENST00000697577.1:n.2919+1823C>A (PALD1)
ENST00000697578.1:n.2763+1823C>A (PALD1)
ENST00000441259.2:c.-5G>T (PRF1) MANE Select ENSP00000398568.1:n.-5G>T
ENST00000638674.1:c.-4-1G>T (PRF1) ENSP00000492048.1:n.-4-1G>T
ENST00000639390.1:n.97+1738G>T (PRF1)
ENST00000373209.2:c.-4-1G>T (PRF1) ENSP00000362305.1:n.-4-1G>T
ENST00000441259.1:c.-5G>T (PRF1) ENSP00000398568.1:n.-5G>T
NM_001083116.1:c.-5G>T , LRG_94t1:c.-5G>T (PRF1) NP_001076585.1:n.-5G>T
NM_005041.4:c.-4-1G>T (PRF1) NP_005032.2:n.-4-1G>T
NM_001083116.2:c.-5G>T (PRF1) NP_001076585.1:n.-5G>T
NM_005041.5:c.-4-1G>T (PRF1) NP_005032.2:n.-4-1G>T
NM_001083116.3:c.-5G>T (PRF1) MANE Select NP_001076585.1:n.-5G>T
NM_005041.6:c.-4-1G>T (PRF1) NP_005032.2:n.-4-1G>T