Canonical Allele Identifier: CA2627248947
Gene: NIPA1 HGNC NCBI

Linked Data

gnomAD v4: 15-22786639-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.22786639A>T , CM000677.2:g.22786639A>T GRCh38
NC_000015.9:g.23086429T>A , CM000677.1:g.23086429T>A GRCh37
NC_000015.8:g.20637870T>A NCBI36
NG_009056.1:g.5415A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000337435.8:c.-18A>T ENSP00000337452.4:n.-18A>T
ENST00000437912.6:c.-48+12326A>T ENSP00000393962.2:n.-48+12326A>T
ENST00000560069.5:n.31+391A>T
ENST00000561183.5:c.-48+391A>T ENSP00000453722.1:n.-48+391A>T
NM_001142275.1:c.-48+391A>T NP_001135747.1:n.-48+391A>T
NM_144599.4:c.-18A>T NP_653200.2:n.-18A>T
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