Canonical Allele Identifier: CA369684397

Gene: CLCN1

Linked Data

• dbSNP Id: rs1262557112
• MyVariant Identifiers: chr7:g.143018836A>G (hg19) ; chr7:g.143321743A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321743A>G , CM000669.2:g.143321743A>G	GRCh38
NC_000007.13:g.143018836A>G , CM000669.1:g.143018836A>G	GRCh37
NC_000007.12:g.142728958A>G	NCBI36
NG_009815.1:g.10618A>G
NG_009815.2:g.10618A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.591A>G	ENSP00000498052.2:p.Ile197Met
ENST00000343257.7:c.591A>G MANE Select	ENSP00000339867.2:p.Ile197Met
ENST00000432192.6:c.359A>G
ENST00000455478.6:c.45A>G	ENSP00000400027.2:p.Ile15Met
ENST00000650516.1:c.591A>G	ENSP00000498052.1:p.Ile197Met
ENST00000343257.6:c.591A>G	ENSP00000339867.2:p.Ile197Met
ENST00000432192.5:c.49A>G
ENST00000455478.5:c.49A>G
ENST00000495612.1:n.49A>G
NM_000083.2:c.591A>G	NP_000074.2:p.Ile197Met
NR_046453.1:n.678A>G
XM_011515781.1:c.591A>G	XP_011514083.1:p.Ile197Met
XM_017011739.1:c.298A>G	XP_016867228.1:p.Thr100Ala
XM_017011740.1:c.298A>G	XP_016867229.1:p.Thr100Ala
NM_000083.3:c.591A>G MANE Select	NP_000074.3:p.Ile197Met
NR_046453.2:n.693A>G