Canonical Allele Identifier: CA1748888152

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321421T= , CM000669.2:g.143321421T=	GRCh38
NC_000007.13:g.143018514T= , CM000669.1:g.143018514T=	GRCh37
NC_000007.12:g.142728636T=	NCBI36
NG_009815.1:g.10296T=
NG_009815.2:g.10296T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.490T=	ENSP00000498052.2:p.Trp164=
ENST00000343257.7:c.490T= MANE Select	ENSP00000339867.2:p.Trp164=
ENST00000432192.6:c.258T=
ENST00000650516.1:c.490T=	ENSP00000498052.1:p.Trp164=
ENST00000343257.6:c.490T=	ENSP00000339867.2:p.Trp164=
NM_000083.2:c.490T=	NP_000074.2:p.Trp164=
NR_046453.1:n.577T=
XM_011515781.1:c.490T=	XP_011514083.1:p.Trp164=
XM_017011739.1:c.197T=	XP_016867228.1:p.Leu66=
XM_017011740.1:c.197T=	XP_016867229.1:p.Leu66=
NM_000083.3:c.490T= MANE Select	NP_000074.3:p.Trp164=
NR_046453.2:n.592T=