Canonical Allele Identifier: CA2163910494
Gene: NIPA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.22786592A= , CM000677.2:g.22786592A= GRCh38
NC_000015.9:g.23086476T= , CM000677.1:g.23086476T= GRCh37
NC_000015.8:g.20637917T= NCBI36
NG_009056.1:g.5368A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000437912.6:c.-48+12279A= ENSP00000393962.2:n.-48+12279A=
ENST00000560069.5:n.31+344A=
ENST00000561183.5:c.-48+344A= ENSP00000453722.1:n.-48+344A=
NM_001142275.1:c.-48+344A= NP_001135747.1:n.-48+344A=