Canonical Allele Identifier: CA1748888923

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143330841C= , CM000669.2:g.143330841C=	GRCh38
NC_000007.13:g.143027934C= , CM000669.1:g.143027934C=	GRCh37
NC_000007.12:g.142738056C=	NCBI36
NG_009815.1:g.19716C=
NG_009815.2:g.19716C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.923C=	ENSP00000498052.2:p.Ala308=
ENST00000343257.7:c.923C= MANE Select	ENSP00000339867.2:p.Ala308=
ENST00000432192.6:c.747C=
ENST00000455478.6:c.511C=	ENSP00000400027.2:n.511C=
ENST00000650516.1:c.923C=	ENSP00000498052.1:p.Ala308=
ENST00000343257.6:c.923C=	ENSP00000339867.2:p.Ala308=
ENST00000432192.5:c.437C=
ENST00000455478.5:c.515C=
ENST00000495612.1:n.224C=
NM_000083.2:c.923C=	NP_000074.2:p.Ala308=
NR_046453.1:n.1013C=
XM_011515781.1:c.923C=	XP_011514083.1:p.Ala308=
XM_017011739.1:c.473C=	XP_016867228.1:p.Ala158=
XM_017011740.1:c.473C=	XP_016867229.1:p.Ala158=
NM_000083.3:c.923C= MANE Select	NP_000074.3:p.Ala308=
NR_046453.2:n.1028C=