Canonical Allele Identifier: CA834507096

Gene: CLCN1

Linked Data

• dbSNP Id: rs1428206522
• gnomAD v4: 7-143321561-T-C
• MyVariant Identifiers: chr7:g.143018654T>C (hg19) ; chr7:g.143321561T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321561T>C , CM000669.2:g.143321561T>C	GRCh38
NC_000007.13:g.143018654T>C , CM000669.1:g.143018654T>C	GRCh37
NC_000007.12:g.142728776T>C	NCBI36
NG_009815.1:g.10436T>C
NG_009815.2:g.10436T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.562+68T>C	ENSP00000498052.2:n.562+68T>C
ENST00000343257.7:c.562+68T>C MANE Select	ENSP00000339867.2:n.562+68T>C
ENST00000432192.6:c.330+68T>C
ENST00000455478.6:c.16+68T>C	ENSP00000400027.2:n.16+68T>C
ENST00000650516.1:c.562+68T>C	ENSP00000498052.1:n.562+68T>C
ENST00000343257.6:c.562+68T>C	ENSP00000339867.2:n.562+68T>C
ENST00000432192.5:c.20+68T>C
ENST00000455478.5:c.20+68T>C
ENST00000495612.1:n.20+68T>C
NM_000083.2:c.562+68T>C	NP_000074.2:n.562+68T>C
NR_046453.1:n.649+68T>C
XM_011515781.1:c.562+68T>C	XP_011514083.1:n.562+68T>C
XM_017011739.1:c.269+68T>C	XP_016867228.1:n.269+68T>C
XM_017011740.1:c.269+68T>C	XP_016867229.1:n.269+68T>C
NM_000083.3:c.562+68T>C MANE Select	NP_000074.3:n.562+68T>C
NR_046453.2:n.664+68T>C