Canonical Allele Identifier: CA458542028

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143018528A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321435A>C , CM000669.2:g.143321435A>C	GRCh38
NC_000007.13:g.143018528A>C , CM000669.1:g.143018528A>C	GRCh37
NC_000007.12:g.142728650A>C	NCBI36
NG_009815.1:g.10310A>C
NG_009815.2:g.10310A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.504A>C	ENSP00000498052.2:p.Pro168=
ENST00000343257.7:c.504A>C MANE Select	ENSP00000339867.2:p.Pro168=
ENST00000432192.6:c.272A>C
ENST00000650516.1:c.504A>C	ENSP00000498052.1:p.Pro168=
ENST00000343257.6:c.504A>C	ENSP00000339867.2:p.Pro168=
NM_000083.2:c.504A>C	NP_000074.2:p.Pro168=
NR_046453.1:n.591A>C
XM_011515781.1:c.504A>C	XP_011514083.1:p.Pro168=
XM_017011739.1:c.211A>C	XP_016867228.1:p.Thr71Pro
XM_017011740.1:c.211A>C	XP_016867229.1:p.Thr71Pro
NM_000083.3:c.504A>C MANE Select	NP_000074.3:p.Pro168=
NR_046453.2:n.606A>C