Canonical Allele Identifier: CA2415190534

Gene: CLCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.10213734G= , CM000685.2:g.10213734G=	GRCh38
NC_000023.10:g.10181774G= , CM000685.1:g.10181774G=	GRCh37
NC_000023.9:g.10141774G=	NCBI36
NG_012496.1:g.61790G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001830.4:c.1630G= MANE Select	NP_001821.2:p.Gly544=
ENST00000380833.9:c.1630G= MANE Select	ENSP00000370213.4:p.Gly544=
NM_001256944.1:c.1348G=	NP_001243873.1:p.Gly450=
NM_001256944.2:c.1348G=	NP_001243873.1:p.Gly450=
NM_001830.3:c.1630G=	NP_001821.2:p.Gly544=
ENST00000380829.5:c.1537G=	ENSP00000370209.1:p.Gly513=
ENST00000380833.8:c.1630G=	ENSP00000370213.4:p.Gly544=
ENST00000421085.6:c.1348G=	ENSP00000405754.2:p.Gly450=
ENST00000421085.7:c.1654G=	ENSP00000405754.3:p.Gly552=
ENST00000674669.1:c.1348G=	ENSP00000501922.1:p.Gly450=
ENST00000675144.1:c.*1404G=	ENSP00000501600.1:n.*1404G=
ENST00000675769.1:c.1630G=	ENSP00000502110.1:p.Gly544=