Canonical Allele Identifier: CA2322133219
Gene: PIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.9838476G= , CM000681.2:g.9838476G= GRCh38
NC_000019.9:g.9949152G= , CM000681.1:g.9949152G= GRCh37
NC_000019.8:g.9810152G= NCBI36
NG_029167.1:g.8270G= , LRG_847:g.8270G=

Transcript Alleles

HGVS Amino-acid Change
NM_006221.4:c.99G= MANE Select NP_006212.1:p.Gln33=
ENST00000247970.9:c.99G= MANE Select ENSP00000247970.5:p.Gln33=
NM_006221.3:c.99G= , LRG_847t1:c.99G= NP_006212.1:p.Gln33=
NR_038422.2:n.290G=
NR_038422.3:n.179G=
NR_038830.1:n.290G=
NR_038830.2:n.179G=
ENST00000247970.8:c.99G= ENSP00000247970.4:p.Gln33=
ENST00000380889.6:n.1132G=
ENST00000585442.5:n.237G=
ENST00000586025.5:n.3146G=
ENST00000586352.5:c.162G=
ENST00000587625.5:c.99G= ENSP00000466656.1:p.Gln33=
ENST00000588695.5:c.99G= ENSP00000466962.1:p.Gln33=
ENST00000589058.5:n.128G=
ENST00000590540.5:n.157G=
XM_011528068.1:c.114G= XP_011526370.1:p.Gln38=
XM_011528068.2:c.114G= XP_011526370.1:p.Gln38=