Canonical Allele Identifier: CA470280032

Gene: PALD1 PRF1

Linked Data

• MyVariant Identifiers: chr10:g.72358676G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70598920G>C , CM000672.2:g.70598920G>C	GRCh38
NC_000010.10:g.72358676G>C , CM000672.1:g.72358676G>C	GRCh37
NC_000010.9:g.72028682G>C	NCBI36
NG_009615.1:g.8856C>G , LRG_94:g.8856C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697571.1:c.2451G>C (PALD1)	ENSP00000513342.1:p.Met817Ile
ENST00000697572.1:c.2250+34401G>C (PALD1)	ENSP00000513343.1:n.2250+34401G>C
ENST00000697573.1:c.2295G>C (PALD1)	ENSP00000513344.1:p.Met765Ile
ENST00000697577.1:n.2755G>C (PALD1)
ENST00000697578.1:n.2599G>C (PALD1)
ENST00000441259.2:c.801C>G (PRF1) MANE Select	ENSP00000398568.1:p.Gly267=
ENST00000638674.1:c.540-1079C>G (PRF1)	ENSP00000492048.1:n.540-1079C>G
ENST00000639390.1:n.98-1079C>G (PRF1)
ENST00000373209.2:c.801C>G (PRF1)	ENSP00000362305.1:p.Gly267=
ENST00000441259.1:c.801C>G (PRF1)	ENSP00000398568.1:p.Gly267=
NM_001083116.1:c.801C>G , LRG_94t1:c.801C>G (PRF1)	NP_001076585.1:p.Gly267=
NM_005041.4:c.801C>G (PRF1)	NP_005032.2:p.Gly267=
NM_001083116.2:c.801C>G (PRF1)	NP_001076585.1:p.Gly267=
NM_005041.5:c.801C>G (PRF1)	NP_005032.2:p.Gly267=
NM_001083116.3:c.801C>G (PRF1) MANE Select	NP_001076585.1:p.Gly267=
NM_005041.6:c.801C>G (PRF1)	NP_005032.2:p.Gly267=