Canonical Allele Identifier: CA416362998
Gene: CLCN6 HGNC NCBI
NPPA-AS1 HGNC NCBI
NPPA HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.11907615C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847558C>G , CM000663.2:g.11847558C>G GRCh38
NC_000001.10:g.11907615C>G , CM000663.1:g.11907615C>G GRCh37
NC_000001.9:g.11830202C>G NCBI36
NG_012926.1:g.5226G>C , LRG_751:g.5226G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1962-19C>G (CLCN6) ENSP00000496938.1:n.*1962-19C>G
ENST00000446542.5:n.906C>G (NPPA-AS1)
ENST00000376476.1:c.-27-119G>C (NPPA) ENSP00000365659.1:n.-27-119G>C
ENST00000376480.7:c.123+4G>C (NPPA) MANE Select ENSP00000365663.3:n.123+4G>C
ENST00000610706.1:c.123+4G>C (NPPA) ENSP00000483195.1:n.123+4G>C
NM_006172.3:c.123+4G>C , LRG_751t1:c.123+4G>C (NPPA) NP_006163.1:n.123+4G>C
NR_037806.1:n.1604C>G (NPPA-AS1)
NM_006172.4:c.123+4G>C (NPPA) MANE Select NP_006163.1:n.123+4G>C
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