Canonical Allele Identifier: CA395196448

Gene: NPIPA2 NPIPA1 NPIPA3

Linked Data

• gnomAD v4: 16-14765120-C-T
• MyVariant Identifiers: chr16:g.14858977C>T (hg19) ; chr16:g.14765120C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14765120C>T , CM000678.2:g.14765120C>T	GRCh38
NC_000016.9:g.14858977C>T , CM000678.1:g.14858977C>T	GRCh37
NC_000016.8:g.14766478C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529166.6:c.817C>T (NPIPA2) MANE Select	ENSP00000432029.1:p.His273Tyr
ENST00000529166.5:c.817C>T (NPIPA2)	ENSP00000432029.1:p.His273Tyr
ENST00000553201.1:c.760C>T (NPIPA2)	ENSP00000446882.1:p.His254Tyr
ENST00000618714.4:c.63+14245C>T (NPIPA1)	ENSP00000484994.1:n.63+14245C>T
ENST00000619019.3:c.902-142C>T (NPIPA3)	ENSP00000479725.1:n.902-142C>T
ENST00000621766.4:c.760C>T (NPIPA3)	ENSP00000483111.1:p.His254Tyr
NM_001277324.1:c.760C>T (NPIPA2)	NP_001264253.1:p.His254Tyr
XM_005255489.2:c.760C>T (NPIPA2)	XP_005255546.1:p.His254Tyr
XR_933118.1:n.168+1282G>A
XR_933119.1:n.168+1282G>A
XR_933120.1:n.168+1282G>A
XM_024450381.1:c.904C>T (NPIPA2)	XP_024306149.1:p.His302Tyr
XM_024450382.1:c.904C>T (NPIPA2)	XP_024306150.1:p.His302Tyr
XM_024450383.1:c.904C>T (NPIPA2)	XP_024306151.1:p.His302Tyr
XM_024450384.1:c.841C>T (NPIPA2)	XP_024306152.1:p.His281Tyr
XM_024450385.1:c.817C>T (NPIPA2)	XP_024306153.1:p.His273Tyr
XM_024450386.1:c.817C>T (NPIPA2)	XP_024306154.1:p.His273Tyr
XM_024450387.1:c.904C>T (NPIPA2)	XP_024306155.1:p.His302Tyr
XM_024450388.1:c.772C>T (NPIPA2)	XP_024306156.1:p.His258Tyr
XR_933118.2:n.168+1282G>A
XR_933120.2:n.168+1282G>A
NM_001277324.3:c.760C>T (NPIPA2)	NP_001264253.1:p.His254Tyr
NM_001395485.2:c.817C>T (NPIPA2) MANE Select	NP_001382414.1:p.His273Tyr
NM_001395486.2:c.817C>T (NPIPA2)	NP_001382415.1:p.His273Tyr