Canonical Allele Identifier: CA1153833044

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847642G= , CM000663.2:g.11847642G= GRCh38
NC_000001.10:g.11907699G= , CM000663.1:g.11907699G= GRCh37
NC_000001.9:g.11830286G= NCBI36
NG_012926.1:g.5142C= , LRG_751:g.5142C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*2027G= (CLCN6) ENSP00000496938.1:n.*2027G=
ENST00000446542.5:n.990G= (NPPA-AS1)
ENST00000376476.1:c.-27-203C= (NPPA) ENSP00000365659.1:n.-27-203C=
ENST00000376480.7:c.43C= (NPPA) MANE Select ENSP00000365663.3:p.Leu15=
ENST00000610706.1:c.43C= (NPPA) ENSP00000483195.1:p.Leu15=
NM_006172.3:c.43C= , LRG_751t1:c.43C= (NPPA) NP_006163.1:p.Leu15=
NM_006172.4:c.43C= (NPPA) MANE Select NP_006163.1:p.Leu15=