Canonical Allele Identifier: CA834512578

Gene: CLCN1

Linked Data

• dbSNP Id: rs1469810662
• gnomAD v3: 7-143331431-G-A
• gnomAD v4: 7-143331431-G-A
• MyVariant Identifiers: chr7:g.143028524G>A (hg19) ; chr7:g.143331431G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143331431G>A , CM000669.2:g.143331431G>A	GRCh38
NC_000007.13:g.143028524G>A , CM000669.1:g.143028524G>A	GRCh37
NC_000007.12:g.142738646G>A	NCBI36
NG_009815.1:g.20306G>A
NG_009815.2:g.20306G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1064+115G>A	ENSP00000498052.2:n.1064+115G>A
ENST00000343257.7:c.1064+115G>A MANE Select	ENSP00000339867.2:n.1064+115G>A
ENST00000432192.6:c.888+115G>A
ENST00000343257.6:c.1064+115G>A	ENSP00000339867.2:n.1064+115G>A
NM_000083.2:c.1064+115G>A	NP_000074.2:n.1064+115G>A
NR_046453.1:n.1154+115G>A
XM_011515781.1:c.1064+115G>A	XP_011514083.1:n.1064+115G>A
XM_017011739.1:c.614+115G>A	XP_016867228.1:n.614+115G>A
XM_017011740.1:c.614+115G>A	XP_016867229.1:n.614+115G>A
NM_000083.3:c.1064+115G>A MANE Select	NP_000074.3:n.1064+115G>A
NR_046453.2:n.1169+115G>A