Canonical Allele Identifier: CA1139773856

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11845727T= , CM000663.2:g.11845727T= GRCh38
NC_000001.10:g.11905784T= , CM000663.1:g.11905784T= GRCh37
NC_000001.9:g.11828371T= NCBI36
NG_012926.1:g.7057A= , LRG_751:g.7057A=

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1922T= (CLCN6) ENSP00000496938.1:n.*1922T=
ENST00000446542.5:n.742T= (NPPA-AS1)
ENST00000376480.7:c.*282A= (NPPA) MANE Select ENSP00000365663.3:n.*282A=
ENST00000610706.1:c.*276A= (NPPA) ENSP00000483195.1:n.*276A=
NM_006172.3:c.*282A= , LRG_751t1:c.*282A= (NPPA) NP_006163.1:n.*282A=
NR_037806.1:n.1440T= (NPPA-AS1)
NM_006172.4:c.*282A= (NPPA) MANE Select NP_006163.1:n.*282A=