Canonical Allele Identifier: CA1748892881
Gene: CLCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143339535G= , CM000669.2:g.143339535G= GRCh38
NC_000007.13:g.143036628G= , CM000669.1:g.143036628G= GRCh37
NC_000007.12:g.142746750G= NCBI36
NG_009815.1:g.28410G=
NG_009815.2:g.28410G=

Transcript Alleles

HGVS Amino-acid change
ENST00000650516.2:c.1496G= ENSP00000498052.2:p.Gly499=
ENST00000343257.7:c.1496G= MANE Select ENSP00000339867.2:p.Gly499=
ENST00000432192.6:c.1320G=
ENST00000343257.6:c.1496G= ENSP00000339867.2:p.Gly499=
NM_000083.2:c.1496G= NP_000074.2:p.Gly499=
NR_046453.1:n.1436G=
XM_011515781.1:c.1520G= XP_011514083.1:p.Gly507=
XM_011515782.1:c.242G= XP_011514084.1:p.Gly81=
XM_011515782.2:c.242G= XP_011514084.1:p.Gly81=
XM_017011739.1:c.1070G= XP_016867228.1:p.Gly357=
XM_017011740.1:c.1046G= XP_016867229.1:p.Gly349=
NM_000083.3:c.1496G= MANE Select NP_000074.3:p.Gly499=
NR_046453.2:n.1451G=