Canonical Allele Identifier: CA9180955

Gene: PIN1

Genomic Alleles

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

Transcript Alleles

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