Canonical Allele Identifier: CA1153829839

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11845736T= , CM000663.2:g.11845736T= GRCh38
NC_000001.10:g.11905793T= , CM000663.1:g.11905793T= GRCh37
NC_000001.9:g.11828380T= NCBI36
NG_012926.1:g.7048A= , LRG_751:g.7048A=

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1931T= (CLCN6) ENSP00000496938.1:n.*1931T=
ENST00000446542.5:n.751T= (NPPA-AS1)
ENST00000376480.7:c.*273A= (NPPA) MANE Select ENSP00000365663.3:n.*273A=
ENST00000610706.1:c.*267A= (NPPA) ENSP00000483195.1:n.*267A=
NM_006172.3:c.*273A= , LRG_751t1:c.*273A= (NPPA) NP_006163.1:n.*273A=
NR_037806.1:n.1449T= (NPPA-AS1)
NM_006172.4:c.*273A= (NPPA) MANE Select NP_006163.1:n.*273A=