Canonical Allele Identifier: CA886104704

Gene: CLCN6 NPPA-AS1 NPPA

Linked Data

• dbSNP Id: rs1347231427
• gnomAD v4: 1-11846154-C-T
• MyVariant Identifiers: chr1:g.11906211C>T (hg19) ; chr1:g.11846154C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11846154C>T , CM000663.2:g.11846154C>T	GRCh38
NC_000001.10:g.11906211C>T , CM000663.1:g.11906211C>T	GRCh37
NC_000001.9:g.11828798C>T	NCBI36
NG_012926.1:g.6630G>A , LRG_751:g.6630G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000400892.3:c.*1961+388C>T (CLCN6)	ENSP00000496938.1:n.*1961+388C>T
ENST00000446542.5:n.781+388C>T (NPPA-AS1)
ENST00000376476.1:c.301-140G>A (NPPA)	ENSP00000365659.1:n.301-140G>A
ENST00000376480.7:c.451-140G>A (NPPA) MANE Select	ENSP00000365663.3:n.451-140G>A
ENST00000610706.1:c.451-140G>A (NPPA)	ENSP00000483195.1:n.451-140G>A
NM_006172.3:c.451-140G>A , LRG_751t1:c.451-140G>A (NPPA)	NP_006163.1:n.451-140G>A
NR_037806.1:n.1479+388C>T (NPPA-AS1)
NM_006172.4:c.451-140G>A (NPPA) MANE Select	NP_006163.1:n.451-140G>A