Canonical Allele Identifier: CA2163930236
Gene: NIPA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.22825341A= , CM000677.2:g.22825341A= GRCh38
NC_000015.9:g.23047727T= , CM000677.1:g.23047727T= GRCh37
NC_000015.8:g.20599168T= NCBI36
NG_009056.1:g.44117A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000337435.9:c.*1102A= MANE Select ENSP00000337452.4:n.*1102A=
ENST00000337435.8:c.*1102A= ENSP00000337452.4:n.*1102A=
ENST00000437912.6:c.*1102A= ENSP00000393962.2:n.*1102A=
ENST00000559448.5:c.2064A=
NM_001142275.1:c.*1102A= NP_001135747.1:n.*1102A=
NM_144599.4:c.*1102A= NP_653200.2:n.*1102A=
NM_144599.5:c.*1102A= MANE Select NP_653200.2:n.*1102A=
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