Canonical Allele Identifier: CA369653509

Gene: CLCN1

Linked Data

• gnomAD v4: 7-143351634-A-G
• MyVariant Identifiers: chr7:g.143048727A>G (hg19) ; chr7:g.143351634A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351634A>G , CM000669.2:g.143351634A>G	GRCh38
NC_000007.13:g.143048727A>G , CM000669.1:g.143048727A>G	GRCh37
NC_000007.12:g.142758849A>G	NCBI36
NG_009815.1:g.40509A>G
NG_009815.2:g.40509A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.2636A>G	ENSP00000498052.2:p.Gln879Arg
ENST00000343257.7:c.2636A>G MANE Select	ENSP00000339867.2:p.Gln879Arg
ENST00000432192.6:c.2460A>G
ENST00000343257.6:c.2636A>G	ENSP00000339867.2:p.Gln879Arg
NM_000083.2:c.2636A>G	NP_000074.2:p.Gln879Arg
NR_046453.1:n.2576A>G
XM_011515781.1:c.2660A>G	XP_011514083.1:p.Gln887Arg
XM_011515782.1:c.1382A>G	XP_011514084.1:p.Gln461Arg
XM_011515782.2:c.1382A>G	XP_011514084.1:p.Gln461Arg
XM_017011739.1:c.2210A>G	XP_016867228.1:p.Gln737Arg
XM_017011740.1:c.2186A>G	XP_016867229.1:p.Gln729Arg
NM_000083.3:c.2636A>G MANE Select	NP_000074.3:p.Gln879Arg
NR_046453.2:n.2591A>G