Canonical Allele Identifier: CA1748881902

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321843A= , CM000669.2:g.143321843A=	GRCh38
NC_000007.13:g.143018936A= , CM000669.1:g.143018936A=	GRCh37
NC_000007.12:g.142729058A=	NCBI36
NG_009815.1:g.10718A=
NG_009815.2:g.10718A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.691A=	ENSP00000498052.2:p.Lys231=
ENST00000343257.7:c.691A= MANE Select	ENSP00000339867.2:p.Lys231=
ENST00000432192.6:c.459A=
ENST00000455478.6:c.145A=	ENSP00000400027.2:p.Lys49=
ENST00000650516.1:c.691A=	ENSP00000498052.1:p.Lys231=
ENST00000343257.6:c.691A=	ENSP00000339867.2:p.Lys231=
ENST00000432192.5:c.149A=
ENST00000455478.5:c.149A=
ENST00000495612.1:n.149A=
NM_000083.2:c.691A=	NP_000074.2:p.Lys231=
NR_046453.1:n.778A=
XM_011515781.1:c.691A=	XP_011514083.1:p.Lys231=
XM_017011739.1:c.398A=	XP_016867228.1:p.Glu133=
XM_017011740.1:c.398A=	XP_016867229.1:p.Glu133=
NM_000083.3:c.691A= MANE Select	NP_000074.3:p.Lys231=
NR_046453.2:n.793A=