Canonical Allele Identifier: CA1153814193

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847683A= , CM000663.2:g.11847683A= GRCh38
NC_000001.10:g.11907740A= , CM000663.1:g.11907740A= GRCh37
NC_000001.9:g.11830327A= NCBI36
NG_012926.1:g.5101T= , LRG_751:g.5101T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*2068A= (CLCN6) ENSP00000496938.1:n.*2068A=
ENST00000446542.5:n.1031A= (NPPA-AS1)
ENST00000376476.1:c.-27-244T= (NPPA) ENSP00000365659.1:n.-27-244T=
ENST00000376480.7:c.2T= (NPPA) MANE Select ENSP00000365663.3:p.Met1=
ENST00000610706.1:c.2T= (NPPA) ENSP00000483195.1:p.Met1=
NM_006172.3:c.2T= , LRG_751t1:c.2T= (NPPA) NP_006163.1:p.Met1=
NM_006172.4:c.2T= (NPPA) MANE Select NP_006163.1:p.Met1=