Canonical Allele Identifier: CA1748889040

Gene: CLCN1

Linked Data

• dbSNP Id: rs1364220599

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143331060A>C , CM000669.2:g.143331060A>C	GRCh38
NC_000007.13:g.143028153A>C , CM000669.1:g.143028153A>C	GRCh37
NC_000007.12:g.142738275A>C	NCBI36
NG_009815.1:g.19935A>C
NG_009815.2:g.19935A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.979+163A>C	ENSP00000498052.2:n.979+163A>C
ENST00000343257.7:c.979+163A>C MANE Select	ENSP00000339867.2:n.979+163A>C
ENST00000432192.6:c.803+163A>C
ENST00000343257.6:c.979+163A>C	ENSP00000339867.2:n.979+163A>C
NM_000083.2:c.979+163A>C	NP_000074.2:n.979+163A>C
NR_046453.1:n.1069+163A>C
XM_011515781.1:c.979+163A>C	XP_011514083.1:n.979+163A>C
XM_017011739.1:c.529+163A>C	XP_016867228.1:n.529+163A>C
XM_017011740.1:c.529+163A>C	XP_016867229.1:n.529+163A>C
NM_000083.3:c.979+163A>C MANE Select	NP_000074.3:n.979+163A>C
NR_046453.2:n.1084+163A>C