Canonical Allele Identifier: CA369684722

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143018879T>G (hg19) ; chr7:g.143321786T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321786T>G , CM000669.2:g.143321786T>G	GRCh38
NC_000007.13:g.143018879T>G , CM000669.1:g.143018879T>G	GRCh37
NC_000007.12:g.142729001T>G	NCBI36
NG_009815.1:g.10661T>G
NG_009815.2:g.10661T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.634T>G	ENSP00000498052.2:p.Phe212Val
ENST00000343257.7:c.634T>G MANE Select	ENSP00000339867.2:p.Phe212Val
ENST00000432192.6:c.402T>G
ENST00000455478.6:c.88T>G	ENSP00000400027.2:p.Phe30Val
ENST00000650516.1:c.634T>G	ENSP00000498052.1:p.Phe212Val
ENST00000343257.6:c.634T>G	ENSP00000339867.2:p.Phe212Val
ENST00000432192.5:c.92T>G
ENST00000455478.5:c.92T>G
ENST00000495612.1:n.92T>G
NM_000083.2:c.634T>G	NP_000074.2:p.Phe212Val
NR_046453.1:n.721T>G
XM_011515781.1:c.634T>G	XP_011514083.1:p.Phe212Val
XM_017011739.1:c.341T>G	XP_016867228.1:p.Leu114Arg
XM_017011740.1:c.341T>G	XP_016867229.1:p.Leu114Arg
NM_000083.3:c.634T>G MANE Select	NP_000074.3:p.Phe212Val
NR_046453.2:n.736T>G