Canonical Allele Identifier: CA1153814241

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847702G= , CM000663.2:g.11847702G= GRCh38
NC_000001.10:g.11907759G= , CM000663.1:g.11907759G= GRCh37
NC_000001.9:g.11830346G= NCBI36
NG_012926.1:g.5082C= , LRG_751:g.5082C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*2087G= (CLCN6) ENSP00000496938.1:n.*2087G=
ENST00000376476.1:c.-27-263C= (NPPA) ENSP00000365659.1:n.-27-263C=
ENST00000376480.7:c.-18C= (NPPA) MANE Select ENSP00000365663.3:n.-18C=
ENST00000610706.1:c.-18C= (NPPA) ENSP00000483195.1:n.-18C=
NM_006172.3:c.-18C= , LRG_751t1:c.-18C= (NPPA) NP_006163.1:n.-18C=
NM_006172.4:c.-18C= (NPPA) MANE Select NP_006163.1:n.-18C=