Canonical Allele Identifier: CA1748898253

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351630G= , CM000669.2:g.143351630G=	GRCh38
NC_000007.13:g.143048723G= , CM000669.1:g.143048723G=	GRCh37
NC_000007.12:g.142758845G=	NCBI36
NG_009815.1:g.40505G=
NG_009815.2:g.40505G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2632G=	ENSP00000498052.2:p.Val878=
ENST00000343257.7:c.2632G= MANE Select	ENSP00000339867.2:p.Val878=
ENST00000432192.6:c.2456G=
ENST00000343257.6:c.2632G=	ENSP00000339867.2:p.Val878=
NM_000083.2:c.2632G=	NP_000074.2:p.Val878=
NR_046453.1:n.2572G=
XM_011515781.1:c.2656G=	XP_011514083.1:p.Val886=
XM_011515782.1:c.1378G=	XP_011514084.1:p.Val460=
XM_011515782.2:c.1378G=	XP_011514084.1:p.Val460=
XM_017011739.1:c.2206G=	XP_016867228.1:p.Val736=
XM_017011740.1:c.2182G=	XP_016867229.1:p.Val728=
NM_000083.3:c.2632G= MANE Select	NP_000074.3:p.Val878=
NR_046453.2:n.2587G=