Canonical Allele Identifier: CA369687537

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143324448G>T , CM000669.2:g.143324448G>T	GRCh38
NC_000007.13:g.143021541G>T , CM000669.1:g.143021541G>T	GRCh37
NC_000007.12:g.142731663G>T	NCBI36
NG_009815.1:g.13323G>T
NG_009815.2:g.13323G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000083.3:c.809G>T MANE Select	NP_000074.3:p.Gly270Val
ENST00000343257.7:c.809G>T MANE Select	ENSP00000339867.2:p.Gly270Val
NM_000083.2:c.809G>T	NP_000074.2:p.Gly270Val
NR_046453.1:n.899G>T
NR_046453.2:n.914G>T
ENST00000343257.6:c.809G>T	ENSP00000339867.2:p.Gly270Val
ENST00000432192.5:c.323G>T
ENST00000432192.6:c.633G>T
ENST00000455478.5:c.401G>T
ENST00000455478.6:c.397G>T	ENSP00000400027.2:n.397G>T
ENST00000495612.1:n.154+2600G>T
ENST00000650516.1:c.853+551G>T	ENSP00000498052.1:n.853+551G>T
ENST00000650516.2:c.853+551G>T	ENSP00000498052.2:n.853+551G>T
XM_011515781.1:c.853+551G>T	XP_011514083.1:n.853+551G>T
XM_017011739.1:c.403+2600G>T	XP_016867228.1:n.403+2600G>T
XM_017011740.1:c.403+2600G>T	XP_016867229.1:n.403+2600G>T