Canonical Allele Identifier: CA2163910533
Gene: NIPA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.22786624C= , CM000677.2:g.22786624C= GRCh38
NC_000015.9:g.23086444G= , CM000677.1:g.23086444G= GRCh37
NC_000015.8:g.20637885G= NCBI36
NG_009056.1:g.5400C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000437912.6:c.-48+12311C= ENSP00000393962.2:n.-48+12311C=
ENST00000560069.5:n.31+376C=
ENST00000561183.5:c.-48+376C= ENSP00000453722.1:n.-48+376C=
NM_001142275.1:c.-48+376C= NP_001135747.1:n.-48+376C=