Canonical Allele Identifier: CA369641656

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143027945A>C (hg19) ; chr7:g.143330852A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143330852A>C , CM000669.2:g.143330852A>C	GRCh38
NC_000007.13:g.143027945A>C , CM000669.1:g.143027945A>C	GRCh37
NC_000007.12:g.142738067A>C	NCBI36
NG_009815.1:g.19727A>C
NG_009815.2:g.19727A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.934A>C	ENSP00000498052.2:p.Ser312Arg
ENST00000343257.7:c.934A>C MANE Select	ENSP00000339867.2:p.Ser312Arg
ENST00000432192.6:c.758A>C
ENST00000455478.6:c.522A>C	ENSP00000400027.2:n.522A>C
ENST00000650516.1:c.934A>C	ENSP00000498052.1:p.Ser312Arg
ENST00000343257.6:c.934A>C	ENSP00000339867.2:p.Ser312Arg
ENST00000432192.5:c.448A>C
ENST00000455478.5:c.526A>C
ENST00000495612.1:n.235A>C
NM_000083.2:c.934A>C	NP_000074.2:p.Ser312Arg
NR_046453.1:n.1024A>C
XM_011515781.1:c.934A>C	XP_011514083.1:p.Ser312Arg
XM_017011739.1:c.484A>C	XP_016867228.1:p.Ser162Arg
XM_017011740.1:c.484A>C	XP_016867229.1:p.Ser162Arg
NM_000083.3:c.934A>C MANE Select	NP_000074.3:p.Ser312Arg
NR_046453.2:n.1039A>C