Canonical Allele Identifier: CA1748884065

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143324333C= , CM000669.2:g.143324333C=	GRCh38
NC_000007.13:g.143021426C= , CM000669.1:g.143021426C=	GRCh37
NC_000007.12:g.142731548C=	NCBI36
NG_009815.1:g.13208C=
NG_009815.2:g.13208C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.853+436C=	ENSP00000498052.2:n.853+436C=
ENST00000343257.7:c.775-81C= MANE Select	ENSP00000339867.2:n.775-81C=
ENST00000432192.6:c.599-81C=
ENST00000455478.6:c.363-81C=	ENSP00000400027.2:n.363-81C=
ENST00000650516.1:c.853+436C=	ENSP00000498052.1:n.853+436C=
ENST00000343257.6:c.775-81C=	ENSP00000339867.2:n.775-81C=
ENST00000432192.5:c.289-81C=
ENST00000455478.5:c.367-81C=
ENST00000495612.1:n.154+2485C=
NM_000083.2:c.775-81C=	NP_000074.2:n.775-81C=
NR_046453.1:n.862-78C=
XM_011515781.1:c.853+436C=	XP_011514083.1:n.853+436C=
XM_017011739.1:c.403+2485C=	XP_016867228.1:n.403+2485C=
XM_017011740.1:c.403+2485C=	XP_016867229.1:n.403+2485C=
NM_000083.3:c.775-81C= MANE Select	NP_000074.3:n.775-81C=
NR_046453.2:n.877-78C=