Canonical Allele Identifier: CA369684691

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143018874A>T (hg19) ; chr7:g.143321781A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321781A>T , CM000669.2:g.143321781A>T	GRCh38
NC_000007.13:g.143018874A>T , CM000669.1:g.143018874A>T	GRCh37
NC_000007.12:g.142728996A>T	NCBI36
NG_009815.1:g.10656A>T
NG_009815.2:g.10656A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.629A>T	ENSP00000498052.2:p.Lys210Ile
ENST00000343257.7:c.629A>T MANE Select	ENSP00000339867.2:p.Lys210Ile
ENST00000432192.6:c.397A>T
ENST00000455478.6:c.83A>T	ENSP00000400027.2:p.Lys28Ile
ENST00000650516.1:c.629A>T	ENSP00000498052.1:p.Lys210Ile
ENST00000343257.6:c.629A>T	ENSP00000339867.2:p.Lys210Ile
ENST00000432192.5:c.87A>T
ENST00000455478.5:c.87A>T
ENST00000495612.1:n.87A>T
NM_000083.2:c.629A>T	NP_000074.2:p.Lys210Ile
NR_046453.1:n.716A>T
XM_011515781.1:c.629A>T	XP_011514083.1:p.Lys210Ile
XM_017011739.1:c.336A>T	XP_016867228.1:p.Glu112Asp
XM_017011740.1:c.336A>T	XP_016867229.1:p.Glu112Asp
NM_000083.3:c.629A>T MANE Select	NP_000074.3:p.Lys210Ile
NR_046453.2:n.731A>T