Canonical Allele Identifier: CA1748881516
Gene: CLCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143321648A= , CM000669.2:g.143321648A= GRCh38
NC_000007.13:g.143018741A= , CM000669.1:g.143018741A= GRCh37
NC_000007.12:g.142728863A= NCBI36
NG_009815.1:g.10523A=
NG_009815.2:g.10523A=

Transcript Alleles

HGVS Amino-acid change
ENST00000650516.2:c.563-67A= ENSP00000498052.2:n.563-67A=
ENST00000343257.7:c.563-67A= MANE Select ENSP00000339867.2:n.563-67A=
ENST00000432192.6:c.331-67A=
ENST00000455478.6:c.17-67A= ENSP00000400027.2:n.17-67A=
ENST00000650516.1:c.563-67A= ENSP00000498052.1:n.563-67A=
ENST00000343257.6:c.563-67A= ENSP00000339867.2:n.563-67A=
ENST00000432192.5:c.21-67A=
ENST00000455478.5:c.21-67A=
ENST00000495612.1:n.21-67A=
NM_000083.2:c.563-67A= NP_000074.2:n.563-67A=
NR_046453.1:n.650-67A=
XM_011515781.1:c.563-67A= XP_011514083.1:n.563-67A=
XM_017011739.1:c.270-67A= XP_016867228.1:n.270-67A=
XM_017011740.1:c.270-67A= XP_016867229.1:n.270-67A=
NM_000083.3:c.563-67A= MANE Select NP_000074.3:n.563-67A=
NR_046453.2:n.665-67A=