Canonical Allele Identifier: CA369686762

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143323375G>C , CM000669.2:g.143323375G>C	GRCh38
NC_000007.13:g.143020468G>C , CM000669.1:g.143020468G>C	GRCh37
NC_000007.12:g.142730590G>C	NCBI36
NG_009815.1:g.12250G>C
NG_009815.2:g.12250G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000083.3:c.763G>C MANE Select	NP_000074.3:p.Gly255Arg
ENST00000343257.7:c.763G>C MANE Select	ENSP00000339867.2:p.Gly255Arg
NM_000083.2:c.763G>C	NP_000074.2:p.Gly255Arg
NR_046453.1:n.850G>C
NR_046453.2:n.865G>C
ENST00000343257.6:c.763G>C	ENSP00000339867.2:p.Gly255Arg
ENST00000432192.5:c.155-198G>C
ENST00000432192.6:c.465-198G>C
ENST00000455478.5:c.221G>C
ENST00000455478.6:c.217G>C	ENSP00000400027.2:p.Gly73Arg
ENST00000495612.1:n.154+1527G>C
ENST00000650516.1:c.763G>C	ENSP00000498052.1:p.Gly255Arg
ENST00000650516.2:c.763G>C	ENSP00000498052.2:p.Gly255Arg
XM_011515781.1:c.763G>C	XP_011514083.1:p.Gly255Arg
XM_017011739.1:c.403+1527G>C	XP_016867228.1:n.403+1527G>C
XM_017011740.1:c.403+1527G>C	XP_016867229.1:n.403+1527G>C