Canonical Allele Identifier: CA369653727

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143048835G>A (hg19) ; chr7:g.143351742G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351742G>A , CM000669.2:g.143351742G>A	GRCh38
NC_000007.13:g.143048835G>A , CM000669.1:g.143048835G>A	GRCh37
NC_000007.12:g.142758957G>A	NCBI36
NG_009815.1:g.40617G>A
NG_009815.2:g.40617G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2744G>A	ENSP00000498052.2:p.Gly915Glu
ENST00000343257.7:c.2744G>A MANE Select	ENSP00000339867.2:p.Gly915Glu
ENST00000343257.6:c.2744G>A	ENSP00000339867.2:p.Gly915Glu
NM_000083.2:c.2744G>A	NP_000074.2:p.Gly915Glu
NR_046453.1:n.2684G>A
XM_011515781.1:c.2768G>A	XP_011514083.1:p.Gly923Glu
XM_011515782.1:c.1490G>A	XP_011514084.1:p.Gly497Glu
XM_011515782.2:c.1490G>A	XP_011514084.1:p.Gly497Glu
XM_017011739.1:c.2318G>A	XP_016867228.1:p.Gly773Glu
XM_017011740.1:c.2294G>A	XP_016867229.1:p.Gly765Glu
NM_000083.3:c.2744G>A MANE Select	NP_000074.3:p.Gly915Glu
NR_046453.2:n.2699G>A