Canonical Allele Identifier: CA1139772908

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847546G= , CM000663.2:g.11847546G= GRCh38
NC_000001.10:g.11907603G= , CM000663.1:g.11907603G= GRCh37
NC_000001.9:g.11830190G= NCBI36
NG_012926.1:g.5238C= , LRG_751:g.5238C=

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1962-31G= (CLCN6) ENSP00000496938.1:n.*1962-31G=
ENST00000446542.5:n.894G= (NPPA-AS1)
ENST00000376476.1:c.-27-107C= (NPPA) ENSP00000365659.1:n.-27-107C=
ENST00000376480.7:c.123+16C= (NPPA) MANE Select ENSP00000365663.3:n.123+16C=
ENST00000610706.1:c.123+16C= (NPPA) ENSP00000483195.1:n.123+16C=
NM_006172.3:c.123+16C= , LRG_751t1:c.123+16C= (NPPA) NP_006163.1:n.123+16C=
NR_037806.1:n.1592G= (NPPA-AS1)
NM_006172.4:c.123+16C= (NPPA) MANE Select NP_006163.1:n.123+16C=