Canonical Allele Identifier: CA1748888880

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143330765C= , CM000669.2:g.143330765C=	GRCh38
NC_000007.13:g.143027858C= , CM000669.1:g.143027858C=	GRCh37
NC_000007.12:g.142737980C=	NCBI36
NG_009815.1:g.19640C=
NG_009815.2:g.19640C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.854-7C=	ENSP00000498052.2:n.854-7C=
ENST00000343257.7:c.854-7C= MANE Select	ENSP00000339867.2:n.854-7C=
ENST00000432192.6:c.678-7C=
ENST00000455478.6:c.442-7C=	ENSP00000400027.2:n.442-7C=
ENST00000650516.1:c.854-7C=	ENSP00000498052.1:n.854-7C=
ENST00000343257.6:c.854-7C=	ENSP00000339867.2:n.854-7C=
ENST00000432192.5:c.368-7C=
ENST00000455478.5:c.446-7C=
ENST00000495612.1:n.155-7C=
NM_000083.2:c.854-7C=	NP_000074.2:n.854-7C=
NR_046453.1:n.944-7C=
XM_011515781.1:c.854-7C=	XP_011514083.1:n.854-7C=
XM_017011739.1:c.404-7C=	XP_016867228.1:n.404-7C=
XM_017011740.1:c.404-7C=	XP_016867229.1:n.404-7C=
NM_000083.3:c.854-7C= MANE Select	NP_000074.3:n.854-7C=
NR_046453.2:n.959-7C=