Canonical Allele Identifier: CA338451867

Linked Data

dbSNP Id: rs1205868073
gnomAD v2: 1-11907660-T-A
gnomAD v4: 1-11847603-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847603T>A , CM000663.2:g.11847603T>A GRCh38
NC_000001.10:g.11907660T>A , CM000663.1:g.11907660T>A GRCh37
NC_000001.9:g.11830247T>A NCBI36
NG_012926.1:g.5181A>T , LRG_751:g.5181A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1988T>A (CLCN6) ENSP00000496938.1:n.*1988T>A
ENST00000446542.5:n.951T>A (NPPA-AS1)
ENST00000376476.1:c.-27-164A>T (NPPA) ENSP00000365659.1:n.-27-164A>T
ENST00000376480.7:c.82A>T (NPPA) MANE Select ENSP00000365663.3:p.Met28Leu
ENST00000610706.1:c.82A>T (NPPA) ENSP00000483195.1:p.Met28Leu
NM_006172.3:c.82A>T , LRG_751t1:c.82A>T (NPPA) NP_006163.1:p.Met28Leu
NR_037806.1:n.1649T>A (NPPA-AS1)
NM_006172.4:c.82A>T (NPPA) MANE Select NP_006163.1:p.Met28Leu