Canonical Allele Identifier: CA416362904

Gene: CLCN6 NPPA-AS1 NPPA

Linked Data

• MyVariant Identifiers: chr1:g.11907596T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11847539T>A , CM000663.2:g.11847539T>A	GRCh38
NC_000001.10:g.11907596T>A , CM000663.1:g.11907596T>A	GRCh37
NC_000001.9:g.11830183T>A	NCBI36
NG_012926.1:g.5245A>T , LRG_751:g.5245A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400892.3:c.*1962-38T>A (CLCN6)	ENSP00000496938.1:n.*1962-38T>A
ENST00000446542.5:n.887T>A (NPPA-AS1)
ENST00000376476.1:c.-27-100A>T (NPPA)	ENSP00000365659.1:n.-27-100A>T
ENST00000376480.7:c.123+23A>T (NPPA) MANE Select	ENSP00000365663.3:n.123+23A>T
ENST00000610706.1:c.123+23A>T (NPPA)	ENSP00000483195.1:n.123+23A>T
NM_006172.3:c.123+23A>T , LRG_751t1:c.123+23A>T (NPPA)	NP_006163.1:n.123+23A>T
NR_037806.1:n.1585T>A (NPPA-AS1)
NM_006172.4:c.123+23A>T (NPPA) MANE Select	NP_006163.1:n.123+23A>T