Canonical Allele Identifier: CA1748888888

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143330775T= , CM000669.2:g.143330775T=	GRCh38
NC_000007.13:g.143027868T= , CM000669.1:g.143027868T=	GRCh37
NC_000007.12:g.142737990T=	NCBI36
NG_009815.1:g.19650T=
NG_009815.2:g.19650T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.857T=	ENSP00000498052.2:p.Val286=
ENST00000343257.7:c.857T= MANE Select	ENSP00000339867.2:p.Val286=
ENST00000432192.6:c.681T=
ENST00000455478.6:c.445T=	ENSP00000400027.2:n.445T=
ENST00000650516.1:c.857T=	ENSP00000498052.1:p.Val286=
ENST00000343257.6:c.857T=	ENSP00000339867.2:p.Val286=
ENST00000432192.5:c.371T=
ENST00000455478.5:c.449T=
ENST00000495612.1:n.158T=
NM_000083.2:c.857T=	NP_000074.2:p.Val286=
NR_046453.1:n.947T=
XM_011515781.1:c.857T=	XP_011514083.1:p.Val286=
XM_017011739.1:c.407T=	XP_016867228.1:p.Val136=
XM_017011740.1:c.407T=	XP_016867229.1:p.Val136=
NM_000083.3:c.857T= MANE Select	NP_000074.3:p.Val286=
NR_046453.2:n.962T=