Canonical Allele Identifier: CA1748882150

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143322124T= , CM000669.2:g.143322124T=	GRCh38
NC_000007.13:g.143019217T= , CM000669.1:g.143019217T=	GRCh37
NC_000007.12:g.142729339T=	NCBI36
NG_009815.1:g.10999T=
NG_009815.2:g.10999T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.696+276T=	ENSP00000498052.2:n.696+276T=
ENST00000343257.7:c.696+276T= MANE Select	ENSP00000339867.2:n.696+276T=
ENST00000432192.6:c.464+276T=
ENST00000455478.6:c.150+276T=	ENSP00000400027.2:n.150+276T=
ENST00000650516.1:c.696+276T=	ENSP00000498052.1:n.696+276T=
ENST00000343257.6:c.696+276T=	ENSP00000339867.2:n.696+276T=
ENST00000432192.5:c.154+276T=
ENST00000455478.5:c.154+276T=
ENST00000495612.1:n.154+276T=
NM_000083.2:c.696+276T=	NP_000074.2:n.696+276T=
NR_046453.1:n.783+276T=
XM_011515781.1:c.696+276T=	XP_011514083.1:n.696+276T=
XM_017011739.1:c.403+276T=	XP_016867228.1:n.403+276T=
XM_017011740.1:c.403+276T=	XP_016867229.1:n.403+276T=
NM_000083.3:c.696+276T= MANE Select	NP_000074.3:n.696+276T=
NR_046453.2:n.798+276T=