Canonical Allele Identifier: CA2163910608

Gene: NIPA1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.22786691C= , CM000677.2:g.22786691C=	GRCh38
NC_000015.9:g.23086377G= , CM000677.1:g.23086377G=	GRCh37
NC_000015.8:g.20637818G=	NCBI36
NG_009056.1:g.5467C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000337435.9:c.35C= MANE Select	ENSP00000337452.4:p.Ala12=
ENST00000337435.8:c.35C=	ENSP00000337452.4:p.Ala12=
ENST00000437912.6:c.-48+12378C=	ENSP00000393962.2:n.-48+12378C=
ENST00000560069.5:n.31+443C=
ENST00000561183.5:c.-48+443C=	ENSP00000453722.1:n.-48+443C=
NM_001142275.1:c.-48+443C=	NP_001135747.1:n.-48+443C=
NM_144599.4:c.35C=	NP_653200.2:p.Ala12=
NM_144599.5:c.35C= MANE Select	NP_653200.2:p.Ala12=