Canonical Allele Identifier: CA369641523

Gene: CLCN1

Linked Data

• ClinVar Variation Id: 3024210
• ClinVar RCV Id: RCV003883257
• MyVariant Identifiers: chr7:g.143027882G>T (hg19) ; chr7:g.143330789G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143330789G>T , CM000669.2:g.143330789G>T	GRCh38
NC_000007.13:g.143027882G>T , CM000669.1:g.143027882G>T	GRCh37
NC_000007.12:g.142738004G>T	NCBI36
NG_009815.1:g.19664G>T
NG_009815.2:g.19664G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.871G>T	ENSP00000498052.2:p.Glu291Ter
ENST00000343257.7:c.871G>T MANE Select	ENSP00000339867.2:p.Glu291Ter
ENST00000432192.6:c.695G>T
ENST00000455478.6:c.459G>T	ENSP00000400027.2:n.459G>T
ENST00000650516.1:c.871G>T	ENSP00000498052.1:p.Glu291Ter
ENST00000343257.6:c.871G>T	ENSP00000339867.2:p.Glu291Ter
ENST00000432192.5:c.385G>T
ENST00000455478.5:c.463G>T
ENST00000495612.1:n.172G>T
NM_000083.2:c.871G>T	NP_000074.2:p.Glu291Ter
NR_046453.1:n.961G>T
XM_011515781.1:c.871G>T	XP_011514083.1:p.Glu291Ter
XM_017011739.1:c.421G>T	XP_016867228.1:p.Glu141Ter
XM_017011740.1:c.421G>T	XP_016867229.1:p.Glu141Ter
NM_000083.3:c.871G>T MANE Select	NP_000074.3:p.Glu291Ter
NR_046453.2:n.976G>T