Canonical Allele Identifier: CA1748884302

Gene: CLCN1

Linked Data

• dbSNP Id: rs1586489467

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143324504A>C , CM000669.2:g.143324504A>C	GRCh38
NC_000007.13:g.143021597A>C , CM000669.1:g.143021597A>C	GRCh37
NC_000007.12:g.142731719A>C	NCBI36
NG_009815.1:g.13379A>C
NG_009815.2:g.13379A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.853+607A>C	ENSP00000498052.2:n.853+607A>C
ENST00000343257.7:c.853+12A>C MANE Select	ENSP00000339867.2:n.853+12A>C
ENST00000432192.6:c.677+12A>C
ENST00000455478.6:c.441+12A>C	ENSP00000400027.2:n.441+12A>C
ENST00000650516.1:c.853+607A>C	ENSP00000498052.1:n.853+607A>C
ENST00000343257.6:c.853+12A>C	ENSP00000339867.2:n.853+12A>C
ENST00000432192.5:c.367+12A>C
ENST00000455478.5:c.445+12A>C
ENST00000495612.1:n.154+2656A>C
NM_000083.2:c.853+12A>C	NP_000074.2:n.853+12A>C
NR_046453.1:n.943+12A>C
XM_011515781.1:c.853+607A>C	XP_011514083.1:n.853+607A>C
XM_017011739.1:c.403+2656A>C	XP_016867228.1:n.403+2656A>C
XM_017011740.1:c.403+2656A>C	XP_016867229.1:n.403+2656A>C
NM_000083.3:c.853+12A>C MANE Select	NP_000074.3:n.853+12A>C
NR_046453.2:n.958+12A>C