Canonical Allele Identifier: CA1748888892

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143330781T= , CM000669.2:g.143330781T=	GRCh38
NC_000007.13:g.143027874T= , CM000669.1:g.143027874T=	GRCh37
NC_000007.12:g.142737996T=	NCBI36
NG_009815.1:g.19656T=
NG_009815.2:g.19656T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.863T=	ENSP00000498052.2:p.Phe288=
ENST00000343257.7:c.863T= MANE Select	ENSP00000339867.2:p.Phe288=
ENST00000432192.6:c.687T=
ENST00000455478.6:c.451T=	ENSP00000400027.2:n.451T=
ENST00000650516.1:c.863T=	ENSP00000498052.1:p.Phe288=
ENST00000343257.6:c.863T=	ENSP00000339867.2:p.Phe288=
ENST00000432192.5:c.377T=
ENST00000455478.5:c.455T=
ENST00000495612.1:n.164T=
NM_000083.2:c.863T=	NP_000074.2:p.Phe288=
NR_046453.1:n.953T=
XM_011515781.1:c.863T=	XP_011514083.1:p.Phe288=
XM_017011739.1:c.413T=	XP_016867228.1:p.Phe138=
XM_017011740.1:c.413T=	XP_016867229.1:p.Phe138=
NM_000083.3:c.863T= MANE Select	NP_000074.3:p.Phe288=
NR_046453.2:n.968T=