Canonical Allele Identifier: CA416363072
Gene: CLCN6 HGNC NCBI
NPPA-AS1 HGNC NCBI
NPPA HGNC NCBI

Linked Data

COSMIC: COSM5441861
MyVariant Identifiers: chr1:g.11907706G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847649G>A , CM000663.2:g.11847649G>A GRCh38
NC_000001.10:g.11907706G>A , CM000663.1:g.11907706G>A GRCh37
NC_000001.9:g.11830293G>A NCBI36
NG_012926.1:g.5135C>T , LRG_751:g.5135C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*2034G>A (CLCN6) ENSP00000496938.1:n.*2034G>A
ENST00000446542.5:n.997G>A (NPPA-AS1)
ENST00000376476.1:c.-27-210C>T (NPPA) ENSP00000365659.1:n.-27-210C>T
ENST00000376480.7:c.36C>T (NPPA) MANE Select ENSP00000365663.3:p.Leu12=
ENST00000610706.1:c.36C>T (NPPA) ENSP00000483195.1:p.Leu12=
NM_006172.3:c.36C>T , LRG_751t1:c.36C>T (NPPA) NP_006163.1:p.Leu12=
NM_006172.4:c.36C>T (NPPA) MANE Select NP_006163.1:p.Leu12=
Search 100 bp 5'
Search 100 bp 3'