Canonical Allele Identifier: CA1748898221

Gene: CLCN1

Linked Data

• dbSNP Id: rs576407487
• gnomAD v4: 7-143351553-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351553T>A , CM000669.2:g.143351553T>A	GRCh38
NC_000007.13:g.143048646T>A , CM000669.1:g.143048646T>A	GRCh37
NC_000007.12:g.142758768T>A	NCBI36
NG_009815.1:g.40428T>A
NG_009815.2:g.40428T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.2596-41T>A	ENSP00000498052.2:n.2596-41T>A
ENST00000343257.7:c.2596-41T>A MANE Select	ENSP00000339867.2:n.2596-41T>A
ENST00000432192.6:c.2420-41T>A
ENST00000343257.6:c.2596-41T>A	ENSP00000339867.2:n.2596-41T>A
NM_000083.2:c.2596-41T>A	NP_000074.2:n.2596-41T>A
NR_046453.1:n.2536-41T>A
XM_011515781.1:c.2620-41T>A	XP_011514083.1:n.2620-41T>A
XM_011515782.1:c.1342-41T>A	XP_011514084.1:n.1342-41T>A
XM_011515782.2:c.1342-41T>A	XP_011514084.1:n.1342-41T>A
XM_017011739.1:c.2170-41T>A	XP_016867228.1:n.2170-41T>A
XM_017011740.1:c.2146-41T>A	XP_016867229.1:n.2146-41T>A
NM_000083.3:c.2596-41T>A MANE Select	NP_000074.3:n.2596-41T>A
NR_046453.2:n.2551-41T>A