Canonical Allele Identifier: CA369684887

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143018903A>T (hg19) ; chr7:g.143321810A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321810A>T , CM000669.2:g.143321810A>T	GRCh38
NC_000007.13:g.143018903A>T , CM000669.1:g.143018903A>T	GRCh37
NC_000007.12:g.142729025A>T	NCBI36
NG_009815.1:g.10685A>T
NG_009815.2:g.10685A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.658A>T	ENSP00000498052.2:p.Thr220Ser
ENST00000343257.7:c.658A>T MANE Select	ENSP00000339867.2:p.Thr220Ser
ENST00000432192.6:c.426A>T
ENST00000455478.6:c.112A>T	ENSP00000400027.2:p.Thr38Ser
ENST00000650516.1:c.658A>T	ENSP00000498052.1:p.Thr220Ser
ENST00000343257.6:c.658A>T	ENSP00000339867.2:p.Thr220Ser
ENST00000432192.5:c.116A>T
ENST00000455478.5:c.116A>T
ENST00000495612.1:n.116A>T
NM_000083.2:c.658A>T	NP_000074.2:p.Thr220Ser
NR_046453.1:n.745A>T
XM_011515781.1:c.658A>T	XP_011514083.1:p.Thr220Ser
XM_017011739.1:c.365A>T	XP_016867228.1:p.Asp122Val
XM_017011740.1:c.365A>T	XP_016867229.1:p.Asp122Val
NM_000083.3:c.658A>T MANE Select	NP_000074.3:p.Thr220Ser
NR_046453.2:n.760A>T