Canonical Allele Identifier: CA2532372493

Gene: CLCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11816526T>G , CM000663.2:g.11816526T>G	GRCh38
NC_000001.10:g.11876583T>G , CM000663.1:g.11876583T>G	GRCh37
NC_000001.9:g.11799170T>G	NCBI36
NG_008766.1:g.15377T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346436.11:c.214-89T>G MANE Select	ENSP00000234488.9:n.214-89T>G
ENST00000400892.3:c.214-89T>G	ENSP00000496938.1:n.214-89T>G
ENST00000312413.10:c.148-89T>G	ENSP00000308367.7:n.148-89T>G
ENST00000346436.10:c.214-89T>G	ENSP00000234488.9:n.214-89T>G
ENST00000376490.7:n.214-89T>G
ENST00000376491.7:n.214-89T>G
ENST00000376492.3:n.214-89T>G
ENST00000376496.4:c.214-89T>G	ENSP00000365679.3:n.214-89T>G
ENST00000376497.7:c.214-89T>G	ENSP00000365680.3:n.214-89T>G
NM_001256959.1:c.148-89T>G	NP_001243888.1:n.148-89T>G
NM_001286.3:c.214-89T>G	NP_001277.1:n.214-89T>G
NR_046428.1:n.381-89T>G
NM_001286.4:c.214-89T>G	NP_001277.1:n.214-89T>G
NM_001256959.2:c.148-89T>G	NP_001243888.2:n.148-89T>G
NM_001286.5:c.214-89T>G MANE Select	NP_001277.2:n.214-89T>G
NR_046428.2:n.286-89T>G