Canonical Allele Identifier: CA1141288513

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847690C= , CM000663.2:g.11847690C= GRCh38
NC_000001.10:g.11907747C= , CM000663.1:g.11907747C= GRCh37
NC_000001.9:g.11830334C= NCBI36
NG_012926.1:g.5094G= , LRG_751:g.5094G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*2075C= (CLCN6) ENSP00000496938.1:n.*2075C=
ENST00000376476.1:c.-27-251G= (NPPA) ENSP00000365659.1:n.-27-251G=
ENST00000376480.7:c.-6G= (NPPA) MANE Select ENSP00000365663.3:n.-6G=
ENST00000610706.1:c.-6G= (NPPA) ENSP00000483195.1:n.-6G=
NM_006172.3:c.-6G= , LRG_751t1:c.-6G= (NPPA) NP_006163.1:n.-6G=
NM_006172.4:c.-6G= (NPPA) MANE Select NP_006163.1:n.-6G=