Canonical Allele Identifier: CA2163910554
Gene: NIPA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.22786653C= , CM000677.2:g.22786653C= GRCh38
NC_000015.9:g.23086415G= , CM000677.1:g.23086415G= GRCh37
NC_000015.8:g.20637856G= NCBI36
NG_009056.1:g.5429C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000337435.9:c.-4C= MANE Select ENSP00000337452.4:n.-4C=
ENST00000337435.8:c.-4C= ENSP00000337452.4:n.-4C=
ENST00000437912.6:c.-48+12340C= ENSP00000393962.2:n.-48+12340C=
ENST00000560069.5:n.31+405C=
ENST00000561183.5:c.-48+405C= ENSP00000453722.1:n.-48+405C=
NM_001142275.1:c.-48+405C= NP_001135747.1:n.-48+405C=
NM_144599.4:c.-4C= NP_653200.2:n.-4C=
NM_144599.5:c.-4C= MANE Select NP_653200.2:n.-4C=
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