Canonical Allele Identifier: CA1153831248

Gene: CLCN6 NPPA-AS1 NPPA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11846779C= , CM000663.2:g.11846779C=	GRCh38
NC_000001.10:g.11906836C= , CM000663.1:g.11906836C=	GRCh37
NC_000001.9:g.11829423C=	NCBI36
NG_012926.1:g.6005G= , LRG_751:g.6005G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400892.3:c.*1962-798C= (CLCN6)	ENSP00000496938.1:n.*1962-798C=
ENST00000446542.5:n.782-655C= (NPPA-AS1)
ENST00000376476.1:c.300+334G= (NPPA)	ENSP00000365659.1:n.300+334G=
ENST00000376480.7:c.450+334G= (NPPA) MANE Select	ENSP00000365663.3:n.450+334G=
ENST00000610706.1:c.450+334G= (NPPA)	ENSP00000483195.1:n.450+334G=
NM_006172.3:c.450+334G= , LRG_751t1:c.450+334G= (NPPA)	NP_006163.1:n.450+334G=
NR_037806.1:n.1480-655C= (NPPA-AS1)
NM_006172.4:c.450+334G= (NPPA) MANE Select	NP_006163.1:n.450+334G=