Canonical Allele Identifier: CA1748898287

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351695A= , CM000669.2:g.143351695A=	GRCh38
NC_000007.13:g.143048788A= , CM000669.1:g.143048788A=	GRCh37
NC_000007.12:g.142758910A=	NCBI36
NG_009815.1:g.40570A=
NG_009815.2:g.40570A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2697A=	ENSP00000498052.2:p.Ala899=
ENST00000343257.7:c.2697A= MANE Select	ENSP00000339867.2:p.Ala899=
ENST00000432192.6:c.2521A=
ENST00000343257.6:c.2697A=	ENSP00000339867.2:p.Ala899=
NM_000083.2:c.2697A=	NP_000074.2:p.Ala899=
NR_046453.1:n.2637A=
XM_011515781.1:c.2721A=	XP_011514083.1:p.Ala907=
XM_011515782.1:c.1443A=	XP_011514084.1:p.Ala481=
XM_011515782.2:c.1443A=	XP_011514084.1:p.Ala481=
XM_017011739.1:c.2271A=	XP_016867228.1:p.Ala757=
XM_017011740.1:c.2247A=	XP_016867229.1:p.Ala749=
NM_000083.3:c.2697A= MANE Select	NP_000074.3:p.Ala899=
NR_046453.2:n.2652A=