Canonical Allele Identifier: CA369687511

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143021528A>G (hg19) ; chr7:g.143324435A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143324435A>G , CM000669.2:g.143324435A>G	GRCh38
NC_000007.13:g.143021528A>G , CM000669.1:g.143021528A>G	GRCh37
NC_000007.12:g.142731650A>G	NCBI36
NG_009815.1:g.13310A>G
NG_009815.2:g.13310A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.853+538A>G	ENSP00000498052.2:n.853+538A>G
ENST00000343257.7:c.796A>G MANE Select	ENSP00000339867.2:p.Ile266Val
ENST00000432192.6:c.620A>G
ENST00000455478.6:c.384A>G	ENSP00000400027.2:n.384A>G
ENST00000650516.1:c.853+538A>G	ENSP00000498052.1:n.853+538A>G
ENST00000343257.6:c.796A>G	ENSP00000339867.2:p.Ile266Val
ENST00000432192.5:c.310A>G
ENST00000455478.5:c.388A>G
ENST00000495612.1:n.154+2587A>G
NM_000083.2:c.796A>G	NP_000074.2:p.Ile266Val
NR_046453.1:n.886A>G
XM_011515781.1:c.853+538A>G	XP_011514083.1:n.853+538A>G
XM_017011739.1:c.403+2587A>G	XP_016867228.1:n.403+2587A>G
XM_017011740.1:c.403+2587A>G	XP_016867229.1:n.403+2587A>G
NM_000083.3:c.796A>G MANE Select	NP_000074.3:p.Ile266Val
NR_046453.2:n.901A>G