Canonical Allele Identifier: CA18010960

Linked Data

dbSNP Id: rs887585085
gnomAD v4: 1-11847597-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847597T>C , CM000663.2:g.11847597T>C GRCh38
NC_000001.10:g.11907654T>C , CM000663.1:g.11907654T>C GRCh37
NC_000001.9:g.11830241T>C NCBI36
NG_012926.1:g.5187A>G , LRG_751:g.5187A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1982T>C (CLCN6) ENSP00000496938.1:n.*1982T>C
ENST00000446542.5:n.945T>C (NPPA-AS1)
ENST00000376476.1:c.-27-158A>G (NPPA) ENSP00000365659.1:n.-27-158A>G
ENST00000376480.7:c.88A>G (NPPA) MANE Select ENSP00000365663.3:p.Asn30Asp
ENST00000610706.1:c.88A>G (NPPA) ENSP00000483195.1:p.Asn30Asp
NM_006172.3:c.88A>G , LRG_751t1:c.88A>G (NPPA) NP_006163.1:p.Asn30Asp
NR_037806.1:n.1643T>C (NPPA-AS1)
NM_006172.4:c.88A>G (NPPA) MANE Select NP_006163.1:p.Asn30Asp