Canonical Allele Identifier: CA1153831791

Linked Data

ClinVar Variation Id: 2965141
ClinVar RCV Id: RCV003823307
dbSNP Id: rs1557442690
gnomAD v4: 1-11847097-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847097C>T , CM000663.2:g.11847097C>T GRCh38
NC_000001.10:g.11907154C>T , CM000663.1:g.11907154C>T GRCh37
NC_000001.9:g.11829741C>T NCBI36
NG_012926.1:g.5687G>A , LRG_751:g.5687G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*1962-480C>T (CLCN6) ENSP00000496938.1:n.*1962-480C>T
ENST00000446542.5:n.782-337C>T (NPPA-AS1)
ENST00000376476.1:c.300+16G>A (NPPA) ENSP00000365659.1:n.300+16G>A
ENST00000376480.7:c.450+16G>A (NPPA) MANE Select ENSP00000365663.3:n.450+16G>A
ENST00000610706.1:c.450+16G>A (NPPA) ENSP00000483195.1:n.450+16G>A
NM_006172.3:c.450+16G>A , LRG_751t1:c.450+16G>A (NPPA) NP_006163.1:n.450+16G>A
NR_037806.1:n.1480-337C>T (NPPA-AS1)
NM_006172.4:c.450+16G>A (NPPA) MANE Select NP_006163.1:n.450+16G>A