Canonical Allele Identifier: CA2643311411

Linked Data

gnomAD v4: 1-11846994-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11846994C>T , CM000663.2:g.11846994C>T GRCh38
NC_000001.10:g.11907051C>T , CM000663.1:g.11907051C>T GRCh37
NC_000001.9:g.11829638C>T NCBI36
NG_012926.1:g.5790G>A , LRG_751:g.5790G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*1962-583C>T (CLCN6) ENSP00000496938.1:n.*1962-583C>T
ENST00000446542.5:n.782-440C>T (NPPA-AS1)
ENST00000376476.1:c.300+119G>A (NPPA) ENSP00000365659.1:n.300+119G>A
ENST00000376480.7:c.450+119G>A (NPPA) MANE Select ENSP00000365663.3:n.450+119G>A
ENST00000610706.1:c.450+119G>A (NPPA) ENSP00000483195.1:n.450+119G>A
NM_006172.3:c.450+119G>A , LRG_751t1:c.450+119G>A (NPPA) NP_006163.1:n.450+119G>A
NR_037806.1:n.1480-440C>T (NPPA-AS1)
NM_006172.4:c.450+119G>A (NPPA) MANE Select NP_006163.1:n.450+119G>A