Canonical Allele Identifier: CA376957991

Gene: PALD1 PRF1

Linked Data

• dbSNP Id: rs1271079313
• gnomAD v2: 10-72358584-T-C
• gnomAD v4: 10-70598828-T-C
• MyVariant Identifiers: chr10:g.72358584T>C (hg19) ; chr10:g.70598828T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70598828T>C , CM000672.2:g.70598828T>C	GRCh38
NC_000010.10:g.72358584T>C , CM000672.1:g.72358584T>C	GRCh37
NC_000010.9:g.72028590T>C	NCBI36
NG_009615.1:g.8948A>G , LRG_94:g.8948A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697571.1:c.2419-60T>C (PALD1)	ENSP00000513342.1:n.2419-60T>C
ENST00000697572.1:c.2250+34309T>C (PALD1)	ENSP00000513343.1:n.2250+34309T>C
ENST00000697573.1:c.2263-60T>C (PALD1)	ENSP00000513344.1:n.2263-60T>C
ENST00000697577.1:n.2723-60T>C (PALD1)
ENST00000697578.1:n.2567-60T>C (PALD1)
ENST00000441259.2:c.893A>G (PRF1) MANE Select	ENSP00000398568.1:p.Glu298Gly
ENST00000638674.1:c.540-987A>G (PRF1)	ENSP00000492048.1:n.540-987A>G
ENST00000639390.1:n.98-987A>G (PRF1)
ENST00000373209.2:c.893A>G (PRF1)	ENSP00000362305.1:p.Glu298Gly
ENST00000441259.1:c.893A>G (PRF1)	ENSP00000398568.1:p.Glu298Gly
NM_001083116.1:c.893A>G , LRG_94t1:c.893A>G (PRF1)	NP_001076585.1:p.Glu298Gly
NM_005041.4:c.893A>G (PRF1)	NP_005032.2:p.Glu298Gly
NM_001083116.2:c.893A>G (PRF1)	NP_001076585.1:p.Glu298Gly
NM_005041.5:c.893A>G (PRF1)	NP_005032.2:p.Glu298Gly
NM_001083116.3:c.893A>G (PRF1) MANE Select	NP_001076585.1:p.Glu298Gly
NM_005041.6:c.893A>G (PRF1)	NP_005032.2:p.Glu298Gly