Canonical Allele Identifier: CA416107498
Gene: CLCN6 HGNC NCBI
NPPA-AS1 HGNC NCBI
NPPA HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.11907170C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847113C>G , CM000663.2:g.11847113C>G GRCh38
NC_000001.10:g.11907170C>G , CM000663.1:g.11907170C>G GRCh37
NC_000001.9:g.11829757C>G NCBI36
NG_012926.1:g.5671G>C , LRG_751:g.5671G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*1962-464C>G (CLCN6) ENSP00000496938.1:n.*1962-464C>G
ENST00000446542.5:n.782-321C>G (NPPA-AS1)
ENST00000376476.1:c.300G>C (NPPA) ENSP00000365659.1:p.Arg100=
ENST00000376480.7:c.450G>C (NPPA) MANE Select ENSP00000365663.3:p.Arg150=
ENST00000610706.1:c.450G>C (NPPA) ENSP00000483195.1:p.Arg150=
NM_006172.3:c.450G>C , LRG_751t1:c.450G>C (NPPA) NP_006163.1:p.Arg150=
NR_037806.1:n.1480-321C>G (NPPA-AS1)
NM_006172.4:c.450G>C (NPPA) MANE Select NP_006163.1:p.Arg150=
Search 100 bp 5'
Search 100 bp 3'