Canonical Allele Identifier: CA2163930234
Gene: NIPA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.22825338G= , CM000677.2:g.22825338G= GRCh38
NC_000015.9:g.23047730C= , CM000677.1:g.23047730C= GRCh37
NC_000015.8:g.20599171C= NCBI36
NG_009056.1:g.44114G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000337435.9:c.*1099G= MANE Select ENSP00000337452.4:n.*1099G=
ENST00000337435.8:c.*1099G= ENSP00000337452.4:n.*1099G=
ENST00000437912.6:c.*1099G= ENSP00000393962.2:n.*1099G=
ENST00000559448.5:c.2061G=
NM_001142275.1:c.*1099G= NP_001135747.1:n.*1099G=
NM_144599.4:c.*1099G= NP_653200.2:n.*1099G=
NM_144599.5:c.*1099G= MANE Select NP_653200.2:n.*1099G=
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