Canonical Allele Identifier: CA369643929
Gene: CLCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143332764A>C , CM000669.2:g.143332764A>C GRCh38
NC_000007.13:g.143029857A>C , CM000669.1:g.143029857A>C GRCh37
NC_000007.12:g.142739979A>C NCBI36
NG_009815.1:g.21639A>C
NG_009815.2:g.21639A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000650516.2:c.1292A>C ENSP00000498052.2:p.Asn431Thr
ENST00000343257.7:c.1292A>C MANE Select ENSP00000339867.2:p.Asn431Thr
ENST00000432192.6:c.1116A>C
ENST00000343257.6:c.1292A>C ENSP00000339867.2:p.Asn431Thr
NM_000083.2:c.1292A>C NP_000074.2:p.Asn431Thr
NR_046453.1:n.1341+261A>C
XM_011515781.1:c.1316A>C XP_011514083.1:p.Asn439Thr
XM_011515782.1:c.38A>C XP_011514084.1:p.Asn13Thr
XM_011515782.2:c.38A>C XP_011514084.1:p.Asn13Thr
XM_017011739.1:c.866A>C XP_016867228.1:p.Asn289Thr
XM_017011740.1:c.842A>C XP_016867229.1:p.Asn281Thr
NM_000083.3:c.1292A>C MANE Select NP_000074.3:p.Asn431Thr
NR_046453.2:n.1356+261A>C