Canonical Allele Identifier: CA458282872

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143036405G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143339312G>T , CM000669.2:g.143339312G>T	GRCh38
NC_000007.13:g.143036405G>T , CM000669.1:g.143036405G>T	GRCh37
NC_000007.12:g.142746527G>T	NCBI36
NG_009815.1:g.28187G>T
NG_009815.2:g.28187G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1461G>T	ENSP00000498052.2:p.Val487=
ENST00000343257.7:c.1461G>T MANE Select	ENSP00000339867.2:p.Val487=
ENST00000432192.6:c.1285G>T
ENST00000343257.6:c.1461G>T	ENSP00000339867.2:p.Val487=
NM_000083.2:c.1461G>T	NP_000074.2:p.Val487=
NR_046453.1:n.1401G>T
XM_011515781.1:c.1485G>T	XP_011514083.1:p.Val495=
XM_011515782.1:c.207G>T	XP_011514084.1:p.Val69=
XM_011515782.2:c.207G>T	XP_011514084.1:p.Val69=
XM_017011739.1:c.1035G>T	XP_016867228.1:p.Val345=
XM_017011740.1:c.1011G>T	XP_016867229.1:p.Val337=
NM_000083.3:c.1461G>T MANE Select	NP_000074.3:p.Val487=
NR_046453.2:n.1416G>T