Canonical Allele Identifier: CA338449322

Linked Data

ClinVar Variation Id: 1446927
ClinVar RCV Id: RCV001987967
dbSNP Id: rs978766447
gnomAD v3: 1-11847191-G-T
gnomAD v4: 1-11847191-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847191G>T , CM000663.2:g.11847191G>T GRCh38
NC_000001.10:g.11907248G>T , CM000663.1:g.11907248G>T GRCh37
NC_000001.9:g.11829835G>T NCBI36
NG_012926.1:g.5593C>A , LRG_751:g.5593C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1962-386G>T (CLCN6) ENSP00000496938.1:n.*1962-386G>T
ENST00000446542.5:n.782-243G>T (NPPA-AS1)
ENST00000376476.1:c.222C>A (NPPA) ENSP00000365659.1:p.Ser74Arg
ENST00000376480.7:c.372C>A (NPPA) MANE Select ENSP00000365663.3:p.Ser124Arg
ENST00000610706.1:c.372C>A (NPPA) ENSP00000483195.1:p.Ser124Arg
NM_006172.3:c.372C>A , LRG_751t1:c.372C>A (NPPA) NP_006163.1:p.Ser124Arg
NR_037806.1:n.1480-243G>T (NPPA-AS1)
NM_006172.4:c.372C>A (NPPA) MANE Select NP_006163.1:p.Ser124Arg