Canonical Allele Identifier: CA898162486

Gene: PDIA5

Linked Data

• dbSNP Id: rs3792366
• gnomAD v3: 3-123121029-G-T
• gnomAD v4: 3-123121029-G-T
• MyVariant Identifiers: chr3:g.122839876G>T (hg19) ; chr3:g.123121029G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123121029G>T , CM000665.2:g.123121029G>T	GRCh38
NC_000003.11:g.122839876G>T , CM000665.1:g.122839876G>T	GRCh37
NC_000003.10:g.124322566G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000316218.12:c.610-3037G>T MANE Select	ENSP00000323313.7:n.610-3037G>T
ENST00000316218.11:c.610-3037G>T	ENSP00000323313.7:n.610-3037G>T
ENST00000489923.5:c.610-3037G>T	ENSP00000417520.1:n.610-3037G>T
NM_006810.3:c.610-3037G>T	NP_006801.1:n.610-3037G>T
NR_028444.1:n.766-3037G>T
XR_427359.1:n.750-3037G>T
XR_427360.1:n.750-3037G>T
NM_006810.4:c.610-3037G>T MANE Select	NP_006801.1:n.610-3037G>T
NR_028444.2:n.750-3037G>T