Canonical Allele Identifier: CA597028
Gene: CLCN6 HGNC NCBI
NPPA-AS1 HGNC NCBI
NPPA HGNC NCBI

Linked Data

ClinVar Variation Id: 2779344
ClinVar RCV Id: RCV003631367
dbSNP Id: rs749463507
ExAC: 1:11907293 G / A
gnomAD v2: 1-11907293-G-A
gnomAD v3: 1-11847236-G-A
gnomAD v4: 1-11847236-G-A
MyVariant Identifiers: chr1:g.11907293G>A (hg19) chr1:g.11847236G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847236G>A , CM000663.2:g.11847236G>A GRCh38
NC_000001.10:g.11907293G>A , CM000663.1:g.11907293G>A GRCh37
NC_000001.9:g.11829880G>A NCBI36
NG_012926.1:g.5548C>T , LRG_751:g.5548C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*1962-341G>A (CLCN6) ENSP00000496938.1:n.*1962-341G>A
ENST00000446542.5:n.782-198G>A (NPPA-AS1)
ENST00000376476.1:c.177C>T (NPPA) ENSP00000365659.1:p.Ala59=
ENST00000376480.7:c.327C>T (NPPA) MANE Select ENSP00000365663.3:p.Ala109=
ENST00000610706.1:c.327C>T (NPPA) ENSP00000483195.1:p.Ala109=
NM_006172.3:c.327C>T , LRG_751t1:c.327C>T (NPPA) NP_006163.1:p.Ala109=
NR_037806.1:n.1480-198G>A (NPPA-AS1)
NM_006172.4:c.327C>T (NPPA) MANE Select NP_006163.1:p.Ala109=
Search 100 bp 5'
Search 100 bp 3'