Canonical Allele Identifier: CA458296248

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143021539G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143324446G>C , CM000669.2:g.143324446G>C	GRCh38
NC_000007.13:g.143021539G>C , CM000669.1:g.143021539G>C	GRCh37
NC_000007.12:g.142731661G>C	NCBI36
NG_009815.1:g.13321G>C
NG_009815.2:g.13321G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.853+549G>C	ENSP00000498052.2:n.853+549G>C
ENST00000343257.7:c.807G>C MANE Select	ENSP00000339867.2:p.Val269=
ENST00000432192.6:c.631G>C
ENST00000455478.6:c.395G>C	ENSP00000400027.2:n.395G>C
ENST00000650516.1:c.853+549G>C	ENSP00000498052.1:n.853+549G>C
ENST00000343257.6:c.807G>C	ENSP00000339867.2:p.Val269=
ENST00000432192.5:c.321G>C
ENST00000455478.5:c.399G>C
ENST00000495612.1:n.154+2598G>C
NM_000083.2:c.807G>C	NP_000074.2:p.Val269=
NR_046453.1:n.897G>C
XM_011515781.1:c.853+549G>C	XP_011514083.1:n.853+549G>C
XM_017011739.1:c.403+2598G>C	XP_016867228.1:n.403+2598G>C
XM_017011740.1:c.403+2598G>C	XP_016867229.1:n.403+2598G>C
NM_000083.3:c.807G>C MANE Select	NP_000074.3:p.Val269=
NR_046453.2:n.912G>C