Canonical Allele Identifier: CA458542083

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143018830G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321737G>A , CM000669.2:g.143321737G>A	GRCh38
NC_000007.13:g.143018830G>A , CM000669.1:g.143018830G>A	GRCh37
NC_000007.12:g.142728952G>A	NCBI36
NG_009815.1:g.10612G>A
NG_009815.2:g.10612G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.585G>A	ENSP00000498052.2:p.Lys195=
ENST00000343257.7:c.585G>A MANE Select	ENSP00000339867.2:p.Lys195=
ENST00000432192.6:c.353G>A
ENST00000455478.6:c.39G>A	ENSP00000400027.2:p.Lys13=
ENST00000650516.1:c.585G>A	ENSP00000498052.1:p.Lys195=
ENST00000343257.6:c.585G>A	ENSP00000339867.2:p.Lys195=
ENST00000432192.5:c.43G>A
ENST00000455478.5:c.43G>A
ENST00000495612.1:n.43G>A
NM_000083.2:c.585G>A	NP_000074.2:p.Lys195=
NR_046453.1:n.672G>A
XM_011515781.1:c.585G>A	XP_011514083.1:p.Lys195=
XM_017011739.1:c.292G>A	XP_016867228.1:p.Asp98Asn
XM_017011740.1:c.292G>A	XP_016867229.1:p.Asp98Asn
NM_000083.3:c.585G>A MANE Select	NP_000074.3:p.Lys195=
NR_046453.2:n.687G>A