Canonical Allele Identifier: CA338449231

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847186C>A , CM000663.2:g.11847186C>A GRCh38
NC_000001.10:g.11907243C>A , CM000663.1:g.11907243C>A GRCh37
NC_000001.9:g.11829830C>A NCBI36
NG_012926.1:g.5598G>T , LRG_751:g.5598G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1962-391C>A (CLCN6) ENSP00000496938.1:n.*1962-391C>A
ENST00000446542.5:n.782-248C>A (NPPA-AS1)
ENST00000376476.1:c.227G>T (NPPA) ENSP00000365659.1:p.Arg76Leu
ENST00000376480.7:c.377G>T (NPPA) MANE Select ENSP00000365663.3:p.Arg126Leu
ENST00000610706.1:c.377G>T (NPPA) ENSP00000483195.1:p.Arg126Leu
NM_006172.3:c.377G>T , LRG_751t1:c.377G>T (NPPA) NP_006163.1:p.Arg126Leu
NR_037806.1:n.1480-248C>A (NPPA-AS1)
NM_006172.4:c.377G>T (NPPA) MANE Select NP_006163.1:p.Arg126Leu