Canonical Allele Identifier: CA369641525

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143027883A>G (hg19) ; chr7:g.143330790A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143330790A>G , CM000669.2:g.143330790A>G	GRCh38
NC_000007.13:g.143027883A>G , CM000669.1:g.143027883A>G	GRCh37
NC_000007.12:g.142738005A>G	NCBI36
NG_009815.1:g.19665A>G
NG_009815.2:g.19665A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.872A>G	ENSP00000498052.2:p.Glu291Gly
ENST00000343257.7:c.872A>G MANE Select	ENSP00000339867.2:p.Glu291Gly
ENST00000432192.6:c.696A>G
ENST00000455478.6:c.460A>G	ENSP00000400027.2:n.460A>G
ENST00000650516.1:c.872A>G	ENSP00000498052.1:p.Glu291Gly
ENST00000343257.6:c.872A>G	ENSP00000339867.2:p.Glu291Gly
ENST00000432192.5:c.386A>G
ENST00000455478.5:c.464A>G
ENST00000495612.1:n.173A>G
NM_000083.2:c.872A>G	NP_000074.2:p.Glu291Gly
NR_046453.1:n.962A>G
XM_011515781.1:c.872A>G	XP_011514083.1:p.Glu291Gly
XM_017011739.1:c.422A>G	XP_016867228.1:p.Glu141Gly
XM_017011740.1:c.422A>G	XP_016867229.1:p.Glu141Gly
NM_000083.3:c.872A>G MANE Select	NP_000074.3:p.Glu291Gly
NR_046453.2:n.977A>G