Canonical Allele Identifier: CA1748898305

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351733A= , CM000669.2:g.143351733A=	GRCh38
NC_000007.13:g.143048826A= , CM000669.1:g.143048826A=	GRCh37
NC_000007.12:g.142758948A=	NCBI36
NG_009815.1:g.40608A=
NG_009815.2:g.40608A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2735A=	ENSP00000498052.2:p.Asp912=
ENST00000343257.7:c.2735A= MANE Select	ENSP00000339867.2:p.Asp912=
ENST00000432192.6:c.2559A=
ENST00000343257.6:c.2735A=	ENSP00000339867.2:p.Asp912=
NM_000083.2:c.2735A=	NP_000074.2:p.Asp912=
NR_046453.1:n.2675A=
XM_011515781.1:c.2759A=	XP_011514083.1:p.Asp920=
XM_011515782.1:c.1481A=	XP_011514084.1:p.Asp494=
XM_011515782.2:c.1481A=	XP_011514084.1:p.Asp494=
XM_017011739.1:c.2309A=	XP_016867228.1:p.Asp770=
XM_017011740.1:c.2285A=	XP_016867229.1:p.Asp762=
NM_000083.3:c.2735A= MANE Select	NP_000074.3:p.Asp912=
NR_046453.2:n.2690A=