Canonical Allele Identifier: CA886104624

Linked Data

dbSNP Id: rs1210930218
gnomAD v3: 1-11845963-G-T
gnomAD v4: 1-11845963-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11845963G>T , CM000663.2:g.11845963G>T GRCh38
NC_000001.10:g.11906020G>T , CM000663.1:g.11906020G>T GRCh37
NC_000001.9:g.11828607G>T NCBI36
NG_012926.1:g.6821C>A , LRG_751:g.6821C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1961+197G>T (CLCN6) ENSP00000496938.1:n.*1961+197G>T
ENST00000446542.5:n.781+197G>T (NPPA-AS1)
ENST00000376476.1:c.*46C>A (NPPA) ENSP00000365659.1:n.*46C>A
ENST00000376480.7:c.*46C>A (NPPA) MANE Select ENSP00000365663.3:n.*46C>A
ENST00000610706.1:c.*40C>A (NPPA) ENSP00000483195.1:n.*40C>A
NM_006172.3:c.*46C>A , LRG_751t1:c.*46C>A (NPPA) NP_006163.1:n.*46C>A
NR_037806.1:n.1479+197G>T (NPPA-AS1)
NM_006172.4:c.*46C>A (NPPA) MANE Select NP_006163.1:n.*46C>A