Canonical Allele Identifier: CA494102382

Gene: NPIPA2 NPIPA1 NPIPA3

Linked Data

• MyVariant Identifiers: chr16:g.14859036C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14765179C>A , CM000678.2:g.14765179C>A	GRCh38
NC_000016.9:g.14859036C>A , CM000678.1:g.14859036C>A	GRCh37
NC_000016.8:g.14766537C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529166.6:c.876C>A (NPIPA2) MANE Select	ENSP00000432029.1:p.Pro292=
ENST00000529166.5:c.876C>A (NPIPA2)	ENSP00000432029.1:p.Pro292=
ENST00000553201.1:c.819C>A (NPIPA2)	ENSP00000446882.1:p.Pro273=
ENST00000618714.4:c.63+14304C>A (NPIPA1)	ENSP00000484994.1:n.63+14304C>A
ENST00000619019.3:c.902-83C>A (NPIPA3)	ENSP00000479725.1:n.902-83C>A
ENST00000621766.4:c.819C>A (NPIPA3)	ENSP00000483111.1:p.Pro273=
NM_001277324.1:c.819C>A (NPIPA2)	NP_001264253.1:p.Pro273=
XM_005255489.2:c.819C>A (NPIPA2)	XP_005255546.1:p.Pro273=
XR_933118.1:n.168+1223G>T
XR_933119.1:n.168+1223G>T
XR_933120.1:n.168+1223G>T
XM_024450381.1:c.963C>A (NPIPA2)	XP_024306149.1:p.Pro321=
XM_024450382.1:c.963C>A (NPIPA2)	XP_024306150.1:p.Pro321=
XM_024450383.1:c.963C>A (NPIPA2)	XP_024306151.1:p.Pro321=
XM_024450384.1:c.900C>A (NPIPA2)	XP_024306152.1:p.Pro300=
XM_024450385.1:c.876C>A (NPIPA2)	XP_024306153.1:p.Pro292=
XM_024450386.1:c.876C>A (NPIPA2)	XP_024306154.1:p.Pro292=
XM_024450387.1:c.963C>A (NPIPA2)	XP_024306155.1:p.Pro321=
XM_024450388.1:c.831C>A (NPIPA2)	XP_024306156.1:p.Pro277=
XR_933118.2:n.168+1223G>T
XR_933120.2:n.168+1223G>T
NM_001277324.3:c.819C>A (NPIPA2)	NP_001264253.1:p.Pro273=
NM_001395485.2:c.876C>A (NPIPA2) MANE Select	NP_001382414.1:p.Pro292=
NM_001395486.2:c.876C>A (NPIPA2)	NP_001382415.1:p.Pro292=