Canonical Allele Identifier: CA1748881430

Gene: CLCN1

Linked Data

• dbSNP Id: rs1802435030

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321549del , CM000669.2:g.143321549del	GRCh38
NC_000007.13:g.143018642del , CM000669.1:g.143018642del	GRCh37
NC_000007.12:g.142728764del	NCBI36
NG_009815.1:g.10424del
NG_009815.2:g.10424del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.562+56del	ENSP00000498052.2:n.562+56del
ENST00000343257.7:c.562+56del MANE Select	ENSP00000339867.2:n.562+56del
ENST00000432192.6:c.330+56del
ENST00000455478.6:c.16+56del	ENSP00000400027.2:n.16+56del
ENST00000650516.1:c.562+56del	ENSP00000498052.1:n.562+56del
ENST00000343257.6:c.562+56del	ENSP00000339867.2:n.562+56del
ENST00000432192.5:c.20+56del
ENST00000455478.5:c.20+56del
ENST00000495612.1:n.20+56del
NM_000083.2:c.562+56del	NP_000074.2:n.562+56del
NR_046453.1:n.649+56del
XM_011515781.1:c.562+56del	XP_011514083.1:n.562+56del
XM_017011739.1:c.269+56del	XP_016867228.1:n.269+56del
XM_017011740.1:c.269+56del	XP_016867229.1:n.269+56del
NM_000083.3:c.562+56del MANE Select	NP_000074.3:n.562+56del
NR_046453.2:n.664+56del