Canonical Allele Identifier: CA1748888864

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143330723A= , CM000669.2:g.143330723A=	GRCh38
NC_000007.13:g.143027816A= , CM000669.1:g.143027816A=	GRCh37
NC_000007.12:g.142737938A=	NCBI36
NG_009815.1:g.19598A=
NG_009815.2:g.19598A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.854-49A=	ENSP00000498052.2:n.854-49A=
ENST00000343257.7:c.854-49A= MANE Select	ENSP00000339867.2:n.854-49A=
ENST00000432192.6:c.678-49A=
ENST00000455478.6:c.442-49A=	ENSP00000400027.2:n.442-49A=
ENST00000650516.1:c.854-49A=	ENSP00000498052.1:n.854-49A=
ENST00000343257.6:c.854-49A=	ENSP00000339867.2:n.854-49A=
ENST00000432192.5:c.368-49A=
ENST00000455478.5:c.446-49A=
ENST00000495612.1:n.155-49A=
NM_000083.2:c.854-49A=	NP_000074.2:n.854-49A=
NR_046453.1:n.944-49A=
XM_011515781.1:c.854-49A=	XP_011514083.1:n.854-49A=
XM_017011739.1:c.404-49A=	XP_016867228.1:n.404-49A=
XM_017011740.1:c.404-49A=	XP_016867229.1:n.404-49A=
NM_000083.3:c.854-49A= MANE Select	NP_000074.3:n.854-49A=
NR_046453.2:n.959-49A=