Canonical Allele Identifier: CA369646346

Gene: CLCN1

Linked Data

• dbSNP Id: rs1803087519
• MyVariant Identifiers: chr7:g.143039024G>A (hg19) ; chr7:g.143341931G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143341931G>A , CM000669.2:g.143341931G>A	GRCh38
NC_000007.13:g.143039024G>A , CM000669.1:g.143039024G>A	GRCh37
NC_000007.12:g.142749146G>A	NCBI36
NG_009815.1:g.30806G>A
NG_009815.2:g.30806G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1585G>A	ENSP00000498052.2:p.Ala529Thr
ENST00000343257.7:c.1585G>A MANE Select	ENSP00000339867.2:p.Ala529Thr
ENST00000432192.6:c.1409G>A
ENST00000343257.6:c.1585G>A	ENSP00000339867.2:p.Ala529Thr
NM_000083.2:c.1585G>A	NP_000074.2:p.Ala529Thr
NR_046453.1:n.1525G>A
XM_011515781.1:c.1609G>A	XP_011514083.1:p.Ala537Thr
XM_011515782.1:c.331G>A	XP_011514084.1:p.Ala111Thr
XM_011515782.2:c.331G>A	XP_011514084.1:p.Ala111Thr
XM_017011739.1:c.1159G>A	XP_016867228.1:p.Ala387Thr
XM_017011740.1:c.1135G>A	XP_016867229.1:p.Ala379Thr
NM_000083.3:c.1585G>A MANE Select	NP_000074.3:p.Ala529Thr
NR_046453.2:n.1540G>A