Canonical Allele Identifier: CA1748898216
Gene: CLCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143351542T= , CM000669.2:g.143351542T= GRCh38
NC_000007.13:g.143048635T= , CM000669.1:g.143048635T= GRCh37
NC_000007.12:g.142758757T= NCBI36
NG_009815.1:g.40417T=
NG_009815.2:g.40417T=

Transcript Alleles

HGVS Amino-acid change
ENST00000650516.2:c.2596-52T= ENSP00000498052.2:n.2596-52T=
ENST00000343257.7:c.2596-52T= MANE Select ENSP00000339867.2:n.2596-52T=
ENST00000432192.6:c.2420-52T=
ENST00000343257.6:c.2596-52T= ENSP00000339867.2:n.2596-52T=
NM_000083.2:c.2596-52T= NP_000074.2:n.2596-52T=
NR_046453.1:n.2536-52T=
XM_011515781.1:c.2620-52T= XP_011514083.1:n.2620-52T=
XM_011515782.1:c.1342-52T= XP_011514084.1:n.1342-52T=
XM_011515782.2:c.1342-52T= XP_011514084.1:n.1342-52T=
XM_017011739.1:c.2170-52T= XP_016867228.1:n.2170-52T=
XM_017011740.1:c.2146-52T= XP_016867229.1:n.2146-52T=
NM_000083.3:c.2596-52T= MANE Select NP_000074.3:n.2596-52T=
NR_046453.2:n.2551-52T=