Canonical Allele Identifier: CA338451798

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847591C>G , CM000663.2:g.11847591C>G GRCh38
NC_000001.10:g.11907648C>G , CM000663.1:g.11907648C>G GRCh37
NC_000001.9:g.11830235C>G NCBI36
NG_012926.1:g.5193G>C , LRG_751:g.5193G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1976C>G (CLCN6) ENSP00000496938.1:n.*1976C>G
ENST00000446542.5:n.939C>G (NPPA-AS1)
ENST00000376476.1:c.-27-152G>C (NPPA) ENSP00000365659.1:n.-27-152G>C
ENST00000376480.7:c.94G>C (NPPA) MANE Select ENSP00000365663.3:p.Val32Leu
ENST00000610706.1:c.94G>C (NPPA) ENSP00000483195.1:p.Val32Leu
NM_006172.3:c.94G>C , LRG_751t1:c.94G>C (NPPA) NP_006163.1:p.Val32Leu
NR_037806.1:n.1637C>G (NPPA-AS1)
NM_006172.4:c.94G>C (NPPA) MANE Select NP_006163.1:p.Val32Leu