Canonical Allele Identifier: CA1748881866

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321822G= , CM000669.2:g.143321822G=	GRCh38
NC_000007.13:g.143018915G= , CM000669.1:g.143018915G=	GRCh37
NC_000007.12:g.142729037G=	NCBI36
NG_009815.1:g.10697G=
NG_009815.2:g.10697G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.670G=	ENSP00000498052.2:p.Gly224=
ENST00000343257.7:c.670G= MANE Select	ENSP00000339867.2:p.Gly224=
ENST00000432192.6:c.438G=
ENST00000455478.6:c.124G=	ENSP00000400027.2:p.Gly42=
ENST00000650516.1:c.670G=	ENSP00000498052.1:p.Gly224=
ENST00000343257.6:c.670G=	ENSP00000339867.2:p.Gly224=
ENST00000432192.5:c.128G=
ENST00000455478.5:c.128G=
ENST00000495612.1:n.128G=
NM_000083.2:c.670G=	NP_000074.2:p.Gly224=
NR_046453.1:n.757G=
XM_011515781.1:c.670G=	XP_011514083.1:p.Gly224=
XM_017011739.1:c.377G=	XP_016867228.1:p.Gly126=
XM_017011740.1:c.377G=	XP_016867229.1:p.Gly126=
NM_000083.3:c.670G= MANE Select	NP_000074.3:p.Gly224=
NR_046453.2:n.772G=