Canonical Allele Identifier: CA2209438002

Gene: NPIPA2 NPIPA1 NPIPA3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14765175C= , CM000678.2:g.14765175C=	GRCh38
NC_000016.9:g.14859032C= , CM000678.1:g.14859032C=	GRCh37
NC_000016.8:g.14766533C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529166.6:c.872C= (NPIPA2) MANE Select	ENSP00000432029.1:p.Thr291=
ENST00000529166.5:c.872C= (NPIPA2)	ENSP00000432029.1:p.Thr291=
ENST00000553201.1:c.815C= (NPIPA2)	ENSP00000446882.1:p.Thr272=
ENST00000618714.4:c.63+14300C= (NPIPA1)	ENSP00000484994.1:n.63+14300C=
ENST00000619019.3:c.902-87C= (NPIPA3)	ENSP00000479725.1:n.902-87C=
ENST00000621766.4:c.815C= (NPIPA3)	ENSP00000483111.1:p.Thr272=
NM_001277324.1:c.815C= (NPIPA2)	NP_001264253.1:p.Thr272=
XM_005255489.2:c.815C= (NPIPA2)	XP_005255546.1:p.Thr272=
XR_933118.1:n.168+1227G=
XR_933119.1:n.168+1227G=
XR_933120.1:n.168+1227G=
XM_024450381.1:c.959C= (NPIPA2)	XP_024306149.1:p.Thr320=
XM_024450382.1:c.959C= (NPIPA2)	XP_024306150.1:p.Thr320=
XM_024450383.1:c.959C= (NPIPA2)	XP_024306151.1:p.Thr320=
XM_024450384.1:c.896C= (NPIPA2)	XP_024306152.1:p.Thr299=
XM_024450385.1:c.872C= (NPIPA2)	XP_024306153.1:p.Thr291=
XM_024450386.1:c.872C= (NPIPA2)	XP_024306154.1:p.Thr291=
XM_024450387.1:c.959C= (NPIPA2)	XP_024306155.1:p.Thr320=
XM_024450388.1:c.827C= (NPIPA2)	XP_024306156.1:p.Thr276=
XR_933118.2:n.168+1227G=
XR_933120.2:n.168+1227G=
NM_001277324.3:c.815C= (NPIPA2)	NP_001264253.1:p.Thr272=
NM_001395485.2:c.872C= (NPIPA2) MANE Select	NP_001382414.1:p.Thr291=
NM_001395486.2:c.872C= (NPIPA2)	NP_001382415.1:p.Thr291=