Canonical Allele Identifier: CA2163910660

Gene: NIPA1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.22786761C= , CM000677.2:g.22786761C=	GRCh38
NC_000015.9:g.23086307G= , CM000677.1:g.23086307G=	GRCh37
NC_000015.8:g.20637748G=	NCBI36
NG_009056.1:g.5537C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337435.9:c.105C= MANE Select	ENSP00000337452.4:p.Ala35=
ENST00000337435.8:c.105C=	ENSP00000337452.4:p.Ala35=
ENST00000437912.6:c.-48+12448C=	ENSP00000393962.2:n.-48+12448C=
ENST00000560069.5:n.31+513C=
ENST00000560105.1:n.4C=
ENST00000561183.5:c.-48+513C=	ENSP00000453722.1:n.-48+513C=
NM_001142275.1:c.-48+513C=	NP_001135747.1:n.-48+513C=
NM_144599.4:c.105C=	NP_653200.2:p.Ala35=
NM_144599.5:c.105C= MANE Select	NP_653200.2:p.Ala35=