Canonical Allele Identifier: CA594704927

Gene: PALD1 PRF1

Linked Data

• dbSNP Id: rs1564723372
• gnomAD v2: 10-72357771-C-CA
• gnomAD v4: 10-70598015-C-CA
• MyVariant Identifiers: chr10:g.72357771_72357772insA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70598016dup , CM000672.2:g.70598016dup	GRCh38
NC_000010.10:g.72357772dup , CM000672.1:g.72357772dup	GRCh37
NC_000010.9:g.72027778dup	NCBI36
NG_009615.1:g.9760dup , LRG_94:g.9760dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697571.1:c.2419-872dup (PALD1)	ENSP00000513342.1:n.2419-872dup
ENST00000697572.1:c.2250+33497dup (PALD1)	ENSP00000513343.1:n.2250+33497dup
ENST00000697573.1:c.2263-872dup (PALD1)	ENSP00000513344.1:n.2263-872dup
ENST00000697577.1:n.2723-872dup (PALD1)
ENST00000697578.1:n.2567-872dup (PALD1)
ENST00000441259.2:c.*37dup (PRF1) MANE Select	ENSP00000398568.1:n.*37dup
ENST00000638674.1:c.540-175dup (PRF1)	ENSP00000492048.1:n.540-175dup
ENST00000639390.1:n.98-175dup (PRF1)
ENST00000373209.2:c.*37dup (PRF1)	ENSP00000362305.1:n.*37dup
ENST00000441259.1:c.*37dup (PRF1)	ENSP00000398568.1:n.*37dup
NM_001083116.1:c.*37dup , LRG_94t1:c.*37dup (PRF1)	NP_001076585.1:n.*37dup
NM_005041.4:c.*37dup (PRF1)	NP_005032.2:n.*37dup
NM_001083116.2:c.*37dup (PRF1)	NP_001076585.1:n.*37dup
NM_005041.5:c.*37dup (PRF1)	NP_005032.2:n.*37dup
NM_001083116.3:c.*37dup (PRF1) MANE Select	NP_001076585.1:n.*37dup
NM_005041.6:c.*37dup (PRF1)	NP_005032.2:n.*37dup