Canonical Allele Identifier: CA2574215433

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847695T>A , CM000663.2:g.11847695T>A GRCh38
NC_000001.10:g.11907752T>A , CM000663.1:g.11907752T>A GRCh37
NC_000001.9:g.11830339T>A NCBI36
NG_012926.1:g.5089A>T , LRG_751:g.5089A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*2080T>A (CLCN6) ENSP00000496938.1:n.*2080T>A
ENST00000376476.1:c.-27-256A>T (NPPA) ENSP00000365659.1:n.-27-256A>T
ENST00000376480.7:c.-11A>T (NPPA) MANE Select ENSP00000365663.3:n.-11A>T
ENST00000610706.1:c.-11A>T (NPPA) ENSP00000483195.1:n.-11A>T
NM_006172.3:c.-11A>T , LRG_751t1:c.-11A>T (NPPA) NP_006163.1:n.-11A>T
NM_006172.4:c.-11A>T (NPPA) MANE Select NP_006163.1:n.-11A>T