Canonical Allele Identifier: CA1153830335

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11846205C= , CM000663.2:g.11846205C= GRCh38
NC_000001.10:g.11906262C= , CM000663.1:g.11906262C= GRCh37
NC_000001.9:g.11828849C= NCBI36
NG_012926.1:g.6579G= , LRG_751:g.6579G=

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1961+439C= (CLCN6) ENSP00000496938.1:n.*1961+439C=
ENST00000446542.5:n.781+439C= (NPPA-AS1)
ENST00000376476.1:c.301-191G= (NPPA) ENSP00000365659.1:n.301-191G=
ENST00000376480.7:c.451-191G= (NPPA) MANE Select ENSP00000365663.3:n.451-191G=
ENST00000610706.1:c.451-191G= (NPPA) ENSP00000483195.1:n.451-191G=
NM_006172.3:c.451-191G= , LRG_751t1:c.451-191G= (NPPA) NP_006163.1:n.451-191G=
NR_037806.1:n.1479+439C= (NPPA-AS1)
NM_006172.4:c.451-191G= (NPPA) MANE Select NP_006163.1:n.451-191G=