Canonical Allele Identifier: CA338448758
Gene: CLCN6 HGNC NCBI
NPPA-AS1 HGNC NCBI
NPPA HGNC NCBI

Linked Data

gnomAD v4: 1-11847138-C-G
MyVariant Identifiers: chr1:g.11907195C>G (hg19) chr1:g.11847138C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847138C>G , CM000663.2:g.11847138C>G GRCh38
NC_000001.10:g.11907195C>G , CM000663.1:g.11907195C>G GRCh37
NC_000001.9:g.11829782C>G NCBI36
NG_012926.1:g.5646G>C , LRG_751:g.5646G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*1962-439C>G (CLCN6) ENSP00000496938.1:n.*1962-439C>G
ENST00000446542.5:n.782-296C>G (NPPA-AS1)
ENST00000376476.1:c.275G>C (NPPA) ENSP00000365659.1:p.Ser92Thr
ENST00000376480.7:c.425G>C (NPPA) MANE Select ENSP00000365663.3:p.Ser142Thr
ENST00000610706.1:c.425G>C (NPPA) ENSP00000483195.1:p.Ser142Thr
NM_006172.3:c.425G>C , LRG_751t1:c.425G>C (NPPA) NP_006163.1:p.Ser142Thr
NR_037806.1:n.1480-296C>G (NPPA-AS1)
NM_006172.4:c.425G>C (NPPA) MANE Select NP_006163.1:p.Ser142Thr
Search 100 bp 5'
Search 100 bp 3'