Canonical Allele Identifier: CA714836377

Gene: PPIB

Linked Data

• dbSNP Id: rs1240003916
• gnomAD v4: 15-64162775-A-AGGGGCTGAGCC
• MyVariant Identifiers: chr15:g.64454974_64454975insGGGGCTGAGCC (hg19) ; chr15:g.64162775_64162776insGGGGCTGAGCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64162776_64162786dup , CM000677.2:g.64162776_64162786dup	GRCh38
NC_000015.9:g.64454975_64454985dup , CM000677.1:g.64454975_64454985dup	GRCh37
NC_000015.8:g.62242028_62242038dup	NCBI36
NG_012979.1:g.5370_5380dup , LRG_10:g.5370_5380dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.135+66_135+76dup MANE Select	ENSP00000300026.4:n.135+66_135+76dup
ENST00000561048.2:n.168+66_168+76dup
ENST00000680158.1:c.135+66_135+76dup	ENSP00000504873.1:n.135+66_135+76dup
ENST00000681397.1:c.135+66_135+76dup	ENSP00000506584.1:n.135+66_135+76dup
ENST00000681658.1:c.30+171_30+181dup	ENSP00000505431.1:n.30+171_30+181dup
ENST00000300026.3:c.135+66_135+76dup	ENSP00000300026.3:n.135+66_135+76dup
ENST00000558492.1:n.155+66_155+76dup
ENST00000561048.1:n.170+66_170+76dup
NM_000942.4:c.135+66_135+76dup , LRG_10t1:c.135+66_135+76dup	NP_000933.1:n.135+66_135+76dup
NM_000942.5:c.135+66_135+76dup MANE Select	NP_000933.1:n.135+66_135+76dup