Canonical Allele Identifier: CA1748893849

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143341779T= , CM000669.2:g.143341779T=	GRCh38
NC_000007.13:g.143038872T= , CM000669.1:g.143038872T=	GRCh37
NC_000007.12:g.142748994T=	NCBI36
NG_009815.1:g.30654T=
NG_009815.2:g.30654T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1583-150T=	ENSP00000498052.2:n.1583-150T=
ENST00000343257.7:c.1583-150T= MANE Select	ENSP00000339867.2:n.1583-150T=
ENST00000432192.6:c.1407-150T=
ENST00000343257.6:c.1583-150T=	ENSP00000339867.2:n.1583-150T=
NM_000083.2:c.1583-150T=	NP_000074.2:n.1583-150T=
NR_046453.1:n.1523-150T=
XM_011515781.1:c.1607-150T=	XP_011514083.1:n.1607-150T=
XM_011515782.1:c.329-150T=	XP_011514084.1:n.329-150T=
XM_011515782.2:c.329-150T=	XP_011514084.1:n.329-150T=
XM_017011739.1:c.1157-150T=	XP_016867228.1:n.1157-150T=
XM_017011740.1:c.1133-150T=	XP_016867229.1:n.1133-150T=
NM_000083.3:c.1583-150T= MANE Select	NP_000074.3:n.1583-150T=
NR_046453.2:n.1538-150T=