Canonical Allele Identifier: CA578446025

Gene: CLCN1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143346954G>A , CM000669.2:g.143346954G>A	GRCh38
NC_000007.13:g.143044047G>A , CM000669.1:g.143044047G>A	GRCh37
NC_000007.12:g.142754169G>A	NCBI36
NG_009815.1:g.35829G>A
NG_009815.2:g.35829G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2403+5G>A	ENSP00000498052.2:n.2403+5G>A
ENST00000343257.7:c.2403+5G>A MANE Select	ENSP00000339867.2:n.2403+5G>A
ENST00000432192.6:c.2227+5G>A
ENST00000343257.6:c.2403+5G>A	ENSP00000339867.2:n.2403+5G>A
NM_000083.2:c.2403+5G>A	NP_000074.2:n.2403+5G>A
NR_046453.1:n.2343+5G>A
XM_011515781.1:c.2427+5G>A	XP_011514083.1:n.2427+5G>A
XM_011515782.1:c.1149+5G>A	XP_011514084.1:n.1149+5G>A
XM_011515782.2:c.1149+5G>A	XP_011514084.1:n.1149+5G>A
XM_017011739.1:c.1977+5G>A	XP_016867228.1:n.1977+5G>A
XM_017011740.1:c.1953+5G>A	XP_016867229.1:n.1953+5G>A
NM_000083.3:c.2403+5G>A MANE Select	NP_000074.3:n.2403+5G>A
NR_046453.2:n.2358+5G>A