Canonical Allele Identifier: CA2627248939
Gene: NIPA1 HGNC NCBI

Linked Data

gnomAD v4: 15-22786634-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.22786634C>A , CM000677.2:g.22786634C>A GRCh38
NC_000015.9:g.23086434G>T , CM000677.1:g.23086434G>T GRCh37
NC_000015.8:g.20637875G>T NCBI36
NG_009056.1:g.5410C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000337435.8:c.-23C>A ENSP00000337452.4:n.-23C>A
ENST00000437912.6:c.-48+12321C>A ENSP00000393962.2:n.-48+12321C>A
ENST00000560069.5:n.31+386C>A
ENST00000561183.5:c.-48+386C>A ENSP00000453722.1:n.-48+386C>A
NM_001142275.1:c.-48+386C>A NP_001135747.1:n.-48+386C>A
NM_144599.4:c.-23C>A NP_653200.2:n.-23C>A
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