Canonical Allele Identifier: CA458296310

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143021575A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143324482A>C , CM000669.2:g.143324482A>C	GRCh38
NC_000007.13:g.143021575A>C , CM000669.1:g.143021575A>C	GRCh37
NC_000007.12:g.142731697A>C	NCBI36
NG_009815.1:g.13357A>C
NG_009815.2:g.13357A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.853+585A>C	ENSP00000498052.2:n.853+585A>C
ENST00000343257.7:c.843A>C MANE Select	ENSP00000339867.2:p.Thr281=
ENST00000432192.6:c.667A>C
ENST00000455478.6:c.431A>C	ENSP00000400027.2:n.431A>C
ENST00000650516.1:c.853+585A>C	ENSP00000498052.1:n.853+585A>C
ENST00000343257.6:c.843A>C	ENSP00000339867.2:p.Thr281=
ENST00000432192.5:c.357A>C
ENST00000455478.5:c.435A>C
ENST00000495612.1:n.154+2634A>C
NM_000083.2:c.843A>C	NP_000074.2:p.Thr281=
NR_046453.1:n.933A>C
XM_011515781.1:c.853+585A>C	XP_011514083.1:n.853+585A>C
XM_017011739.1:c.403+2634A>C	XP_016867228.1:n.403+2634A>C
XM_017011740.1:c.403+2634A>C	XP_016867229.1:n.403+2634A>C
NM_000083.3:c.843A>C MANE Select	NP_000074.3:p.Thr281=
NR_046453.2:n.948A>C