Canonical Allele Identifier: CA714836383

Gene: PPIB

Linked Data

• dbSNP Id: rs1209405445
• MyVariant Identifiers: chr15:g.64454982_64454987del (hg19) ; chr15:g.64162783_64162788del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64162783_64162788del , CM000677.2:g.64162783_64162788del	GRCh38
NC_000015.9:g.64454982_64454987del , CM000677.1:g.64454982_64454987del	GRCh37
NC_000015.8:g.62242035_62242040del	NCBI36
NG_012979.1:g.5368_5373del , LRG_10:g.5368_5373del

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.135+64_135+69del MANE Select	ENSP00000300026.4:n.135+64_135+69del
ENST00000561048.2:n.168+64_168+69del
ENST00000680158.1:c.135+64_135+69del	ENSP00000504873.1:n.135+64_135+69del
ENST00000681397.1:c.135+64_135+69del	ENSP00000506584.1:n.135+64_135+69del
ENST00000681658.1:c.30+169_30+174del	ENSP00000505431.1:n.30+169_30+174del
ENST00000300026.3:c.135+64_135+69del	ENSP00000300026.3:n.135+64_135+69del
ENST00000558492.1:n.155+64_155+69del
ENST00000561048.1:n.170+64_170+69del
NM_000942.4:c.135+64_135+69del , LRG_10t1:c.135+64_135+69del	NP_000933.1:n.135+64_135+69del
NM_000942.5:c.135+64_135+69del MANE Select	NP_000933.1:n.135+64_135+69del