Canonical Allele Identifier: CA2163910576

Gene: NIPA1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.22786669G= , CM000677.2:g.22786669G=	GRCh38
NC_000015.9:g.23086399C= , CM000677.1:g.23086399C=	GRCh37
NC_000015.8:g.20637840C=	NCBI36
NG_009056.1:g.5445G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337435.9:c.13G= MANE Select	ENSP00000337452.4:p.Ala5=
ENST00000337435.8:c.13G=	ENSP00000337452.4:p.Ala5=
ENST00000437912.6:c.-48+12356G=	ENSP00000393962.2:n.-48+12356G=
ENST00000560069.5:n.31+421G=
ENST00000561183.5:c.-48+421G=	ENSP00000453722.1:n.-48+421G=
NM_001142275.1:c.-48+421G=	NP_001135747.1:n.-48+421G=
NM_144599.4:c.13G=	NP_653200.2:p.Ala5=
NM_144599.5:c.13G= MANE Select	NP_653200.2:p.Ala5=