Canonical Allele Identifier: CA338451835

Linked Data

gnomAD v4: 1-11847596-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847596T>G , CM000663.2:g.11847596T>G GRCh38
NC_000001.10:g.11907653T>G , CM000663.1:g.11907653T>G GRCh37
NC_000001.9:g.11830240T>G NCBI36
NG_012926.1:g.5188A>C , LRG_751:g.5188A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1981T>G (CLCN6) ENSP00000496938.1:n.*1981T>G
ENST00000446542.5:n.944T>G (NPPA-AS1)
ENST00000376476.1:c.-27-157A>C (NPPA) ENSP00000365659.1:n.-27-157A>C
ENST00000376480.7:c.89A>C (NPPA) MANE Select ENSP00000365663.3:p.Asn30Thr
ENST00000610706.1:c.89A>C (NPPA) ENSP00000483195.1:p.Asn30Thr
NM_006172.3:c.89A>C , LRG_751t1:c.89A>C (NPPA) NP_006163.1:p.Asn30Thr
NR_037806.1:n.1642T>G (NPPA-AS1)
NM_006172.4:c.89A>C (NPPA) MANE Select NP_006163.1:p.Asn30Thr