Canonical Allele Identifier: CA4537038
Gene: CLCN1 HGNC NCBI

Linked Data

dbSNP Id: rs765869090

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143321858G>A , CM000669.2:g.143321858G>A GRCh38
NC_000007.13:g.143018951G>A , CM000669.1:g.143018951G>A GRCh37
NC_000007.12:g.142729073G>A NCBI36
NG_009815.1:g.10733G>A
NG_009815.2:g.10733G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000650516.2:c.696+10G>A ENSP00000498052.2:n.696+10G>A
ENST00000343257.7:c.696+10G>A MANE Select ENSP00000339867.2:n.696+10G>A
ENST00000432192.6:c.464+10G>A
ENST00000455478.6:c.150+10G>A ENSP00000400027.2:n.150+10G>A
ENST00000650516.1:c.696+10G>A ENSP00000498052.1:n.696+10G>A
ENST00000343257.6:c.696+10G>A ENSP00000339867.2:n.696+10G>A
ENST00000432192.5:c.154+10G>A
ENST00000455478.5:c.154+10G>A
ENST00000495612.1:n.154+10G>A
NM_000083.2:c.696+10G>A NP_000074.2:n.696+10G>A
NR_046453.1:n.783+10G>A
XM_011515781.1:c.696+10G>A XP_011514083.1:n.696+10G>A
XM_017011739.1:c.403+10G>A XP_016867228.1:n.403+10G>A
XM_017011740.1:c.403+10G>A XP_016867229.1:n.403+10G>A
NM_000083.3:c.696+10G>A MANE Select NP_000074.3:n.696+10G>A
NR_046453.2:n.798+10G>A