Canonical Allele Identifier: CA338451821

Linked Data

dbSNP Id: rs1477893541
gnomAD v4: 1-11847594-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847594C>T , CM000663.2:g.11847594C>T GRCh38
NC_000001.10:g.11907651C>T , CM000663.1:g.11907651C>T GRCh37
NC_000001.9:g.11830238C>T NCBI36
NG_012926.1:g.5190G>A , LRG_751:g.5190G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1979C>T (CLCN6) ENSP00000496938.1:n.*1979C>T
ENST00000446542.5:n.942C>T (NPPA-AS1)
ENST00000376476.1:c.-27-155G>A (NPPA) ENSP00000365659.1:n.-27-155G>A
ENST00000376480.7:c.91G>A (NPPA) MANE Select ENSP00000365663.3:p.Ala31Thr
ENST00000610706.1:c.91G>A (NPPA) ENSP00000483195.1:p.Ala31Thr
NM_006172.3:c.91G>A , LRG_751t1:c.91G>A (NPPA) NP_006163.1:p.Ala31Thr
NR_037806.1:n.1640C>T (NPPA-AS1)
NM_006172.4:c.91G>A (NPPA) MANE Select NP_006163.1:p.Ala31Thr