Canonical Allele Identifier: CA391298355
Gene: NIPA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 887002
ClinVar RCV Id: RCV001119480 RCV003227915
dbSNP Id: rs780312828
gnomAD v3: 15-22786705-G-A
gnomAD v4: 15-22786705-G-A
MyVariant Identifiers: chr15:g.23086363C>T (hg19) chr15:g.22786705G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.22786705G>A , CM000677.2:g.22786705G>A GRCh38
NC_000015.9:g.23086363C>T , CM000677.1:g.23086363C>T GRCh37
NC_000015.8:g.20637804C>T NCBI36
NG_009056.1:g.5481G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000337435.9:c.49G>A MANE Select ENSP00000337452.4:p.Gly17Arg
ENST00000337435.8:c.49G>A ENSP00000337452.4:p.Gly17Arg
ENST00000437912.6:c.-48+12392G>A ENSP00000393962.2:n.-48+12392G>A
ENST00000560069.5:n.31+457G>A
ENST00000561183.5:c.-48+457G>A ENSP00000453722.1:n.-48+457G>A
NM_001142275.1:c.-48+457G>A NP_001135747.1:n.-48+457G>A
NM_144599.4:c.49G>A NP_653200.2:p.Gly17Arg
NM_144599.5:c.49G>A MANE Select NP_653200.2:p.Gly17Arg
Search 100 bp 5'
Search 100 bp 3'