Canonical Allele Identifier: CA1748888929

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143330853G= , CM000669.2:g.143330853G=	GRCh38
NC_000007.13:g.143027946G= , CM000669.1:g.143027946G=	GRCh37
NC_000007.12:g.142738068G=	NCBI36
NG_009815.1:g.19728G=
NG_009815.2:g.19728G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.935G=	ENSP00000498052.2:p.Ser312=
ENST00000343257.7:c.935G= MANE Select	ENSP00000339867.2:p.Ser312=
ENST00000432192.6:c.759G=
ENST00000455478.6:c.523G=	ENSP00000400027.2:n.523G=
ENST00000650516.1:c.935G=	ENSP00000498052.1:p.Ser312=
ENST00000343257.6:c.935G=	ENSP00000339867.2:p.Ser312=
ENST00000432192.5:c.449G=
ENST00000455478.5:c.527G=
ENST00000495612.1:n.236G=
NM_000083.2:c.935G=	NP_000074.2:p.Ser312=
NR_046453.1:n.1025G=
XM_011515781.1:c.935G=	XP_011514083.1:p.Ser312=
XM_017011739.1:c.485G=	XP_016867228.1:p.Ser162=
XM_017011740.1:c.485G=	XP_016867229.1:p.Ser162=
NM_000083.3:c.935G= MANE Select	NP_000074.3:p.Ser312=
NR_046453.2:n.1040G=