Canonical Allele Identifier: CA1748889188

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143331394A= , CM000669.2:g.143331394A=	GRCh38
NC_000007.13:g.143028487A= , CM000669.1:g.143028487A=	GRCh37
NC_000007.12:g.142738609A=	NCBI36
NG_009815.1:g.20269A=
NG_009815.2:g.20269A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1064+78A=	ENSP00000498052.2:n.1064+78A=
ENST00000343257.7:c.1064+78A= MANE Select	ENSP00000339867.2:n.1064+78A=
ENST00000432192.6:c.888+78A=
ENST00000343257.6:c.1064+78A=	ENSP00000339867.2:n.1064+78A=
NM_000083.2:c.1064+78A=	NP_000074.2:n.1064+78A=
NR_046453.1:n.1154+78A=
XM_011515781.1:c.1064+78A=	XP_011514083.1:n.1064+78A=
XM_017011739.1:c.614+78A=	XP_016867228.1:n.614+78A=
XM_017011740.1:c.614+78A=	XP_016867229.1:n.614+78A=
NM_000083.3:c.1064+78A= MANE Select	NP_000074.3:n.1064+78A=
NR_046453.2:n.1169+78A=