Canonical Allele Identifier: CA458280543

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143027905T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143330812T>A , CM000669.2:g.143330812T>A	GRCh38
NC_000007.13:g.143027905T>A , CM000669.1:g.143027905T>A	GRCh37
NC_000007.12:g.142738027T>A	NCBI36
NG_009815.1:g.19687T>A
NG_009815.2:g.19687T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.894T>A	ENSP00000498052.2:p.Ala298=
ENST00000343257.7:c.894T>A MANE Select	ENSP00000339867.2:p.Ala298=
ENST00000432192.6:c.718T>A
ENST00000455478.6:c.482T>A	ENSP00000400027.2:n.482T>A
ENST00000650516.1:c.894T>A	ENSP00000498052.1:p.Ala298=
ENST00000343257.6:c.894T>A	ENSP00000339867.2:p.Ala298=
ENST00000432192.5:c.408T>A
ENST00000455478.5:c.486T>A
ENST00000495612.1:n.195T>A
NM_000083.2:c.894T>A	NP_000074.2:p.Ala298=
NR_046453.1:n.984T>A
XM_011515781.1:c.894T>A	XP_011514083.1:p.Ala298=
XM_017011739.1:c.444T>A	XP_016867228.1:p.Ala148=
XM_017011740.1:c.444T>A	XP_016867229.1:p.Ala148=
NM_000083.3:c.894T>A MANE Select	NP_000074.3:p.Ala298=
NR_046453.2:n.999T>A