Canonical Allele Identifier: CA338449370

Linked Data

ClinVar Variation Id: 574575
ClinVar RCV Id: RCV000696540
dbSNP Id: rs1215729892
gnomAD v2: 1-11907250-T-C
gnomAD v4: 1-11847193-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11847193T>C , CM000663.2:g.11847193T>C GRCh38
NC_000001.10:g.11907250T>C , CM000663.1:g.11907250T>C GRCh37
NC_000001.9:g.11829837T>C NCBI36
NG_012926.1:g.5591A>G , LRG_751:g.5591A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1962-384T>C (CLCN6) ENSP00000496938.1:n.*1962-384T>C
ENST00000446542.5:n.782-241T>C (NPPA-AS1)
ENST00000376476.1:c.220A>G (NPPA) ENSP00000365659.1:p.Ser74Gly
ENST00000376480.7:c.370A>G (NPPA) MANE Select ENSP00000365663.3:p.Ser124Gly
ENST00000610706.1:c.370A>G (NPPA) ENSP00000483195.1:p.Ser124Gly
NM_006172.3:c.370A>G , LRG_751t1:c.370A>G (NPPA) NP_006163.1:p.Ser124Gly
NR_037806.1:n.1480-241T>C (NPPA-AS1)
NM_006172.4:c.370A>G (NPPA) MANE Select NP_006163.1:p.Ser124Gly