Canonical Allele Identifier: CA369653282

Gene: CLCN1

Linked Data

• COSMIC: COSM6176869
• MyVariant Identifiers: chr7:g.143047716G>T (hg19) ; chr7:g.143350623G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143350623G>T , CM000669.2:g.143350623G>T	GRCh38
NC_000007.13:g.143047716G>T , CM000669.1:g.143047716G>T	GRCh37
NC_000007.12:g.142757838G>T	NCBI36
NG_009815.1:g.39498G>T
NG_009815.2:g.39498G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2564G>T	ENSP00000498052.2:p.Gly855Val
ENST00000343257.7:c.2564G>T MANE Select	ENSP00000339867.2:p.Gly855Val
ENST00000432192.6:c.2388G>T
ENST00000343257.6:c.2564G>T	ENSP00000339867.2:p.Gly855Val
NM_000083.2:c.2564G>T	NP_000074.2:p.Gly855Val
NR_046453.1:n.2504G>T
XM_011515781.1:c.2588G>T	XP_011514083.1:p.Gly863Val
XM_011515782.1:c.1310G>T	XP_011514084.1:p.Gly437Val
XM_011515782.2:c.1310G>T	XP_011514084.1:p.Gly437Val
XM_017011739.1:c.2138G>T	XP_016867228.1:p.Gly713Val
XM_017011740.1:c.2114G>T	XP_016867229.1:p.Gly705Val
NM_000083.3:c.2564G>T MANE Select	NP_000074.3:p.Gly855Val
NR_046453.2:n.2519G>T