Canonical Allele Identifier: CA2163910517
Gene: NIPA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.22786609G= , CM000677.2:g.22786609G= GRCh38
NC_000015.9:g.23086459C= , CM000677.1:g.23086459C= GRCh37
NC_000015.8:g.20637900C= NCBI36
NG_009056.1:g.5385G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000437912.6:c.-48+12296G= ENSP00000393962.2:n.-48+12296G=
ENST00000560069.5:n.31+361G=
ENST00000561183.5:c.-48+361G= ENSP00000453722.1:n.-48+361G=
NM_001142275.1:c.-48+361G= NP_001135747.1:n.-48+361G=