Canonical Allele Identifier: CA395196492

Gene: NPIPA2 NPIPA1 NPIPA3

Linked Data

• MyVariant Identifiers: chr16:g.14858984T>G (hg19) ; chr16:g.14765127T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14765127T>G , CM000678.2:g.14765127T>G	GRCh38
NC_000016.9:g.14858984T>G , CM000678.1:g.14858984T>G	GRCh37
NC_000016.8:g.14766485T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529166.6:c.824T>G (NPIPA2) MANE Select	ENSP00000432029.1:p.Ile275Arg
ENST00000529166.5:c.824T>G (NPIPA2)	ENSP00000432029.1:p.Ile275Arg
ENST00000553201.1:c.767T>G (NPIPA2)	ENSP00000446882.1:p.Ile256Arg
ENST00000618714.4:c.63+14252T>G (NPIPA1)	ENSP00000484994.1:n.63+14252T>G
ENST00000619019.3:c.902-135T>G (NPIPA3)	ENSP00000479725.1:n.902-135T>G
ENST00000621766.4:c.767T>G (NPIPA3)	ENSP00000483111.1:p.Ile256Arg
NM_001277324.1:c.767T>G (NPIPA2)	NP_001264253.1:p.Ile256Arg
XM_005255489.2:c.767T>G (NPIPA2)	XP_005255546.1:p.Ile256Arg
XR_933118.1:n.168+1275A>C
XR_933119.1:n.168+1275A>C
XR_933120.1:n.168+1275A>C
XM_024450381.1:c.911T>G (NPIPA2)	XP_024306149.1:p.Ile304Arg
XM_024450382.1:c.911T>G (NPIPA2)	XP_024306150.1:p.Ile304Arg
XM_024450383.1:c.911T>G (NPIPA2)	XP_024306151.1:p.Ile304Arg
XM_024450384.1:c.848T>G (NPIPA2)	XP_024306152.1:p.Ile283Arg
XM_024450385.1:c.824T>G (NPIPA2)	XP_024306153.1:p.Ile275Arg
XM_024450386.1:c.824T>G (NPIPA2)	XP_024306154.1:p.Ile275Arg
XM_024450387.1:c.911T>G (NPIPA2)	XP_024306155.1:p.Ile304Arg
XM_024450388.1:c.779T>G (NPIPA2)	XP_024306156.1:p.Ile260Arg
XR_933118.2:n.168+1275A>C
XR_933120.2:n.168+1275A>C
NM_001277324.3:c.767T>G (NPIPA2)	NP_001264253.1:p.Ile256Arg
NM_001395485.2:c.824T>G (NPIPA2) MANE Select	NP_001382414.1:p.Ile275Arg
NM_001395486.2:c.824T>G (NPIPA2)	NP_001382415.1:p.Ile275Arg