Canonical Allele Identifier: CA1748881515
Gene: CLCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143321645C= , CM000669.2:g.143321645C= GRCh38
NC_000007.13:g.143018738C= , CM000669.1:g.143018738C= GRCh37
NC_000007.12:g.142728860C= NCBI36
NG_009815.1:g.10520C=
NG_009815.2:g.10520C=

Transcript Alleles

HGVS Amino-acid change
ENST00000650516.2:c.563-70C= ENSP00000498052.2:n.563-70C=
ENST00000343257.7:c.563-70C= MANE Select ENSP00000339867.2:n.563-70C=
ENST00000432192.6:c.331-70C=
ENST00000455478.6:c.17-70C= ENSP00000400027.2:n.17-70C=
ENST00000650516.1:c.563-70C= ENSP00000498052.1:n.563-70C=
ENST00000343257.6:c.563-70C= ENSP00000339867.2:n.563-70C=
ENST00000432192.5:c.21-70C=
ENST00000455478.5:c.21-70C=
ENST00000495612.1:n.21-70C=
NM_000083.2:c.563-70C= NP_000074.2:n.563-70C=
NR_046453.1:n.650-70C=
XM_011515781.1:c.563-70C= XP_011514083.1:n.563-70C=
XM_017011739.1:c.270-70C= XP_016867228.1:n.270-70C=
XM_017011740.1:c.270-70C= XP_016867229.1:n.270-70C=
NM_000083.3:c.563-70C= MANE Select NP_000074.3:n.563-70C=
NR_046453.2:n.665-70C=