Canonical Allele Identifier: CA1748898437

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143352003G= , CM000669.2:g.143352003G=	GRCh38
NC_000007.13:g.143049096G= , CM000669.1:g.143049096G=	GRCh37
NC_000007.12:g.142759218G=	NCBI36
NG_009815.1:g.40878G=
NG_009815.2:g.40878G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.*38G=	ENSP00000498052.2:n.*38G=
ENST00000343257.7:c.*38G= MANE Select	ENSP00000339867.2:n.*38G=
ENST00000343257.6:c.*38G=	ENSP00000339867.2:n.*38G=
NM_000083.2:c.*38G=	NP_000074.2:n.*38G=
NR_046453.1:n.2945G=
XM_011515781.1:c.*38G=	XP_011514083.1:n.*38G=
XM_011515782.1:c.*38G=	XP_011514084.1:n.*38G=
XM_011515782.2:c.*38G=	XP_011514084.1:n.*38G=
XM_017011739.1:c.*38G=	XP_016867228.1:n.*38G=
XM_017011740.1:c.*38G=	XP_016867229.1:n.*38G=
NM_000083.3:c.*38G= MANE Select	NP_000074.3:n.*38G=
NR_046453.2:n.2960G=