Canonical Allele Identifier: CA1748888932
Gene: CLCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143330862T= , CM000669.2:g.143330862T= GRCh38
NC_000007.13:g.143027955T= , CM000669.1:g.143027955T= GRCh37
NC_000007.12:g.142738077T= NCBI36
NG_009815.1:g.19737T=
NG_009815.2:g.19737T=

Transcript Alleles

HGVS Amino-acid change
ENST00000650516.2:c.944T= ENSP00000498052.2:p.Val315=
ENST00000343257.7:c.944T= MANE Select ENSP00000339867.2:p.Val315=
ENST00000432192.6:c.768T=
ENST00000455478.6:c.532T= ENSP00000400027.2:n.532T=
ENST00000650516.1:c.944T= ENSP00000498052.1:p.Val315=
ENST00000343257.6:c.944T= ENSP00000339867.2:p.Val315=
ENST00000432192.5:c.458T=
ENST00000455478.5:c.536T=
ENST00000495612.1:n.245T=
NM_000083.2:c.944T= NP_000074.2:p.Val315=
NR_046453.1:n.1034T=
XM_011515781.1:c.944T= XP_011514083.1:p.Val315=
XM_017011739.1:c.494T= XP_016867228.1:p.Val165=
XM_017011740.1:c.494T= XP_016867229.1:p.Val165=
NM_000083.3:c.944T= MANE Select NP_000074.3:p.Val315=
NR_046453.2:n.1049T=