Canonical Allele Identifier: CA2643310717

Linked Data

gnomAD v4: 1-11845770-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11845770A>T , CM000663.2:g.11845770A>T GRCh38
NC_000001.10:g.11905827A>T , CM000663.1:g.11905827A>T GRCh37
NC_000001.9:g.11828414A>T NCBI36
NG_012926.1:g.7014T>A , LRG_751:g.7014T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1961+4A>T (CLCN6) ENSP00000496938.1:n.*1961+4A>T
ENST00000446542.5:n.781+4A>T (NPPA-AS1)
ENST00000376480.7:c.*239T>A (NPPA) MANE Select ENSP00000365663.3:n.*239T>A
ENST00000610706.1:c.*233T>A (NPPA) ENSP00000483195.1:n.*233T>A
NM_006172.3:c.*239T>A , LRG_751t1:c.*239T>A (NPPA) NP_006163.1:n.*239T>A
NR_037806.1:n.1479+4A>T (NPPA-AS1)
NM_006172.4:c.*239T>A (NPPA) MANE Select NP_006163.1:n.*239T>A