Canonical Allele Identifier: CA458296263

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143021548T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143324455T>G , CM000669.2:g.143324455T>G	GRCh38
NC_000007.13:g.143021548T>G , CM000669.1:g.143021548T>G	GRCh37
NC_000007.12:g.142731670T>G	NCBI36
NG_009815.1:g.13330T>G
NG_009815.2:g.13330T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.853+558T>G	ENSP00000498052.2:n.853+558T>G
ENST00000343257.7:c.816T>G MANE Select	ENSP00000339867.2:p.Ala272=
ENST00000432192.6:c.640T>G
ENST00000455478.6:c.404T>G	ENSP00000400027.2:n.404T>G
ENST00000650516.1:c.853+558T>G	ENSP00000498052.1:n.853+558T>G
ENST00000343257.6:c.816T>G	ENSP00000339867.2:p.Ala272=
ENST00000432192.5:c.330T>G
ENST00000455478.5:c.408T>G
ENST00000495612.1:n.154+2607T>G
NM_000083.2:c.816T>G	NP_000074.2:p.Ala272=
NR_046453.1:n.906T>G
XM_011515781.1:c.853+558T>G	XP_011514083.1:n.853+558T>G
XM_017011739.1:c.403+2607T>G	XP_016867228.1:n.403+2607T>G
XM_017011740.1:c.403+2607T>G	XP_016867229.1:n.403+2607T>G
NM_000083.3:c.816T>G MANE Select	NP_000074.3:p.Ala272=
NR_046453.2:n.921T>G