Canonical Allele Identifier: CA2685383101
Gene: CLCN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143321642_143321647del , CM000669.2:g.143321642_143321647del GRCh38
NC_000007.13:g.143018735_143018740del , CM000669.1:g.143018735_143018740del GRCh37
NC_000007.12:g.142728857_142728862del NCBI36
NG_009815.1:g.10517_10522del
NG_009815.2:g.10517_10522del

Transcript Alleles

HGVS Amino-acid change
ENST00000650516.2:c.563-73_563-68del ENSP00000498052.2:n.563-73_563-68del
ENST00000343257.7:c.563-73_563-68del MANE Select ENSP00000339867.2:n.563-73_563-68del
ENST00000432192.6:c.331-73_331-68del
ENST00000455478.6:c.17-73_17-68del ENSP00000400027.2:n.17-73_17-68del
ENST00000650516.1:c.563-73_563-68del ENSP00000498052.1:n.563-73_563-68del
ENST00000343257.6:c.563-73_563-68del ENSP00000339867.2:n.563-73_563-68del
ENST00000432192.5:c.21-73_21-68del
ENST00000455478.5:c.21-73_21-68del
ENST00000495612.1:n.21-73_21-68del
NM_000083.2:c.563-73_563-68del NP_000074.2:n.563-73_563-68del
NR_046453.1:n.650-73_650-68del
XM_011515781.1:c.563-73_563-68del XP_011514083.1:n.563-73_563-68del
XM_017011739.1:c.270-73_270-68del XP_016867228.1:n.270-73_270-68del
XM_017011740.1:c.270-73_270-68del XP_016867229.1:n.270-73_270-68del
NM_000083.3:c.563-73_563-68del MANE Select NP_000074.3:n.563-73_563-68del
NR_046453.2:n.665-73_665-68del