Canonical Allele Identifier: CA494102022

Gene: NPIPA2 NPIPA1 NPIPA3

Linked Data

• MyVariant Identifiers: chr16:g.14858898A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14765041A>G , CM000678.2:g.14765041A>G	GRCh38
NC_000016.9:g.14858898A>G , CM000678.1:g.14858898A>G	GRCh37
NC_000016.8:g.14766399A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529166.6:c.738A>G (NPIPA2) MANE Select	ENSP00000432029.1:p.Gly246=
ENST00000529166.5:c.738A>G (NPIPA2)	ENSP00000432029.1:p.Gly246=
ENST00000553201.1:c.681A>G (NPIPA2)	ENSP00000446882.1:p.Gly227=
ENST00000618714.4:c.63+14166A>G (NPIPA1)	ENSP00000484994.1:n.63+14166A>G
ENST00000619019.3:c.902-221A>G (NPIPA3)	ENSP00000479725.1:n.902-221A>G
ENST00000621766.4:c.681A>G (NPIPA3)	ENSP00000483111.1:p.Gly227=
NM_001277324.1:c.681A>G (NPIPA2)	NP_001264253.1:p.Gly227=
XM_005255489.2:c.681A>G (NPIPA2)	XP_005255546.1:p.Gly227=
XM_006720917.2:c.*52A>G (NPIPA2)	XP_006720980.2:n.*52A>G
XR_933118.1:n.168+1361T>C
XR_933119.1:n.168+1361T>C
XR_933120.1:n.168+1361T>C
XM_011522595.2:c.*184A>G (NPIPA2)	XP_011520897.1:n.*184A>G
XM_024450381.1:c.825A>G (NPIPA2)	XP_024306149.1:p.Gly275=
XM_024450382.1:c.825A>G (NPIPA2)	XP_024306150.1:p.Gly275=
XM_024450383.1:c.825A>G (NPIPA2)	XP_024306151.1:p.Gly275=
XM_024450384.1:c.762A>G (NPIPA2)	XP_024306152.1:p.Gly254=
XM_024450385.1:c.738A>G (NPIPA2)	XP_024306153.1:p.Gly246=
XM_024450386.1:c.738A>G (NPIPA2)	XP_024306154.1:p.Gly246=
XM_024450387.1:c.825A>G (NPIPA2)	XP_024306155.1:p.Gly275=
XM_024450388.1:c.693A>G (NPIPA2)	XP_024306156.1:p.Gly231=
XR_933118.2:n.168+1361T>C
XR_933120.2:n.168+1361T>C
NM_001277324.3:c.681A>G (NPIPA2)	NP_001264253.1:p.Gly227=
NM_001395485.2:c.738A>G (NPIPA2) MANE Select	NP_001382414.1:p.Gly246=
NM_001395486.2:c.738A>G (NPIPA2)	NP_001382415.1:p.Gly246=