Canonical Allele Identifier: CA2631866779

Gene: NPIPA2 NPIPA1 NPIPA3

Linked Data

• gnomAD v4: 16-14765113-TCAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.14765119_14765121del , CM000678.2:g.14765119_14765121del	GRCh38
NC_000016.9:g.14858976_14858978del , CM000678.1:g.14858976_14858978del	GRCh37
NC_000016.8:g.14766477_14766479del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529166.6:c.816_818del (NPIPA2) MANE Select	ENSP00000432029.1:p.Gln272del
ENST00000529166.5:c.816_818del (NPIPA2)	ENSP00000432029.1:p.Gln272del
ENST00000553201.1:c.759_761del (NPIPA2)	ENSP00000446882.1:p.Gln253del
ENST00000618714.4:c.63+14244_63+14246del (NPIPA1)	ENSP00000484994.1:n.63+14244_63+14246del
ENST00000619019.3:c.902-143_902-141del (NPIPA3)	ENSP00000479725.1:n.902-143_902-141del
ENST00000621766.4:c.759_761del (NPIPA3)	ENSP00000483111.1:p.Gln253del
NM_001277324.1:c.759_761del (NPIPA2)	NP_001264253.1:p.Gln253del
XM_005255489.2:c.759_761del (NPIPA2)	XP_005255546.1:p.Gln253del
XR_933118.1:n.168+1286_168+1288del
XR_933119.1:n.168+1286_168+1288del
XR_933120.1:n.168+1286_168+1288del
XM_024450381.1:c.903_905del (NPIPA2)	XP_024306149.1:p.Gln301del
XM_024450382.1:c.903_905del (NPIPA2)	XP_024306150.1:p.Gln301del
XM_024450383.1:c.903_905del (NPIPA2)	XP_024306151.1:p.Gln301del
XM_024450384.1:c.840_842del (NPIPA2)	XP_024306152.1:p.Gln280del
XM_024450385.1:c.816_818del (NPIPA2)	XP_024306153.1:p.Gln272del
XM_024450386.1:c.816_818del (NPIPA2)	XP_024306154.1:p.Gln272del
XM_024450387.1:c.903_905del (NPIPA2)	XP_024306155.1:p.Gln301del
XM_024450388.1:c.771_773del (NPIPA2)	XP_024306156.1:p.Gln257del
XR_933118.2:n.168+1286_168+1288del
XR_933120.2:n.168+1286_168+1288del
NM_001277324.3:c.759_761del (NPIPA2)	NP_001264253.1:p.Gln253del
NM_001395485.2:c.816_818del (NPIPA2) MANE Select	NP_001382414.1:p.Gln272del
NM_001395486.2:c.816_818del (NPIPA2)	NP_001382415.1:p.Gln272del