Canonical Allele Identifier: CA369641660

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143027946G>C (hg19) ; chr7:g.143330853G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.935G>C	ENSP00000498052.2:p.Ser312Thr
ENST00000343257.7:c.935G>C MANE Select	ENSP00000339867.2:p.Ser312Thr
ENST00000432192.6:c.759G>C
ENST00000455478.6:c.523G>C	ENSP00000400027.2:n.523G>C
ENST00000650516.1:c.935G>C	ENSP00000498052.1:p.Ser312Thr
ENST00000343257.6:c.935G>C	ENSP00000339867.2:p.Ser312Thr
ENST00000432192.5:c.449G>C
ENST00000455478.5:c.527G>C
ENST00000495612.1:n.236G>C
NM_000083.2:c.935G>C	NP_000074.2:p.Ser312Thr
NR_046453.1:n.1025G>C
XM_011515781.1:c.935G>C	XP_011514083.1:p.Ser312Thr
XM_017011739.1:c.485G>C	XP_016867228.1:p.Ser162Thr
XM_017011740.1:c.485G>C	XP_016867229.1:p.Ser162Thr
NM_000083.3:c.935G>C MANE Select	NP_000074.3:p.Ser312Thr
NR_046453.2:n.1040G>C