Canonical Allele Identifier: CA2209437959

Gene: NPIPA2 NPIPA1 NPIPA3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14765089G= , CM000678.2:g.14765089G=	GRCh38
NC_000016.9:g.14858946G= , CM000678.1:g.14858946G=	GRCh37
NC_000016.8:g.14766447G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529166.6:c.786G= (NPIPA2) MANE Select	ENSP00000432029.1:p.Met262=
ENST00000529166.5:c.786G= (NPIPA2)	ENSP00000432029.1:p.Met262=
ENST00000553201.1:c.729G= (NPIPA2)	ENSP00000446882.1:p.Met243=
ENST00000618714.4:c.63+14214G= (NPIPA1)	ENSP00000484994.1:n.63+14214G=
ENST00000619019.3:c.902-173G= (NPIPA3)	ENSP00000479725.1:n.902-173G=
ENST00000621766.4:c.729G= (NPIPA3)	ENSP00000483111.1:p.Met243=
NM_001277324.1:c.729G= (NPIPA2)	NP_001264253.1:p.Met243=
XM_005255489.2:c.729G= (NPIPA2)	XP_005255546.1:p.Met243=
XM_006720917.2:c.*100G= (NPIPA2)	XP_006720980.2:n.*100G=
XR_933118.1:n.168+1313C=
XR_933119.1:n.168+1313C=
XR_933120.1:n.168+1313C=
XM_011522595.2:c.*232G= (NPIPA2)	XP_011520897.1:n.*232G=
XM_024450381.1:c.873G= (NPIPA2)	XP_024306149.1:p.Met291=
XM_024450382.1:c.873G= (NPIPA2)	XP_024306150.1:p.Met291=
XM_024450383.1:c.873G= (NPIPA2)	XP_024306151.1:p.Met291=
XM_024450384.1:c.810G= (NPIPA2)	XP_024306152.1:p.Met270=
XM_024450385.1:c.786G= (NPIPA2)	XP_024306153.1:p.Met262=
XM_024450386.1:c.786G= (NPIPA2)	XP_024306154.1:p.Met262=
XM_024450387.1:c.873G= (NPIPA2)	XP_024306155.1:p.Met291=
XM_024450388.1:c.741G= (NPIPA2)	XP_024306156.1:p.Met247=
XR_933118.2:n.168+1313C=
XR_933120.2:n.168+1313C=
NM_001277324.3:c.729G= (NPIPA2)	NP_001264253.1:p.Met243=
NM_001395485.2:c.786G= (NPIPA2) MANE Select	NP_001382414.1:p.Met262=
NM_001395486.2:c.786G= (NPIPA2)	NP_001382415.1:p.Met262=