Canonical Allele Identifier: CA5538733

Linked Data

dbSNP Id: rs774467483

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70598243A>G , CM000672.2:g.70598243A>G GRCh38
NC_000010.10:g.72357999A>G , CM000672.1:g.72357999A>G GRCh37
NC_000010.9:g.72028005A>G NCBI36
NG_009615.1:g.9533T>C , LRG_94:g.9533T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000697571.1:c.2419-645A>G (PALD1) ENSP00000513342.1:n.2419-645A>G
ENST00000697572.1:c.2250+33724A>G (PALD1) ENSP00000513343.1:n.2250+33724A>G
ENST00000697573.1:c.2263-645A>G (PALD1) ENSP00000513344.1:n.2263-645A>G
ENST00000697577.1:n.2723-645A>G (PALD1)
ENST00000697578.1:n.2567-645A>G (PALD1)
ENST00000441259.2:c.1478T>C (PRF1) MANE Select ENSP00000398568.1:p.Leu493Pro
ENST00000638674.1:c.540-402T>C (PRF1) ENSP00000492048.1:n.540-402T>C
ENST00000639390.1:n.98-402T>C (PRF1)
ENST00000373209.2:c.1478T>C (PRF1) ENSP00000362305.1:p.Leu493Pro
ENST00000441259.1:c.1478T>C (PRF1) ENSP00000398568.1:p.Leu493Pro
NM_001083116.1:c.1478T>C , LRG_94t1:c.1478T>C (PRF1) NP_001076585.1:p.Leu493Pro
NM_005041.4:c.1478T>C (PRF1) NP_005032.2:p.Leu493Pro
NM_001083116.2:c.1478T>C (PRF1) NP_001076585.1:p.Leu493Pro
NM_005041.5:c.1478T>C (PRF1) NP_005032.2:p.Leu493Pro
NM_001083116.3:c.1478T>C (PRF1) MANE Select NP_001076585.1:p.Leu493Pro
NM_005041.6:c.1478T>C (PRF1) NP_005032.2:p.Leu493Pro