Canonical Allele Identifier: CA2685380762

Gene: CLCN1

Linked Data

• gnomAD v4: 7-143332268-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143332268T>A , CM000669.2:g.143332268T>A	GRCh38
NC_000007.13:g.143029361T>A , CM000669.1:g.143029361T>A	GRCh37
NC_000007.12:g.142739483T>A	NCBI36
NG_009815.1:g.21143T>A
NG_009815.2:g.21143T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1167-151T>A	ENSP00000498052.2:n.1167-151T>A
ENST00000343257.7:c.1167-151T>A MANE Select	ENSP00000339867.2:n.1167-151T>A
ENST00000432192.6:c.991-151T>A
ENST00000343257.6:c.1167-151T>A	ENSP00000339867.2:n.1167-151T>A
NM_000083.2:c.1167-151T>A	NP_000074.2:n.1167-151T>A
NR_046453.1:n.1257-151T>A
XM_011515781.1:c.1167-151T>A	XP_011514083.1:n.1167-151T>A
XM_011515782.1:c.-3-456T>A	XP_011514084.1:n.-3-456T>A
XM_011515782.2:c.-3-456T>A	XP_011514084.1:n.-3-456T>A
XM_017011739.1:c.717-151T>A	XP_016867228.1:n.717-151T>A
XM_017011740.1:c.717-151T>A	XP_016867229.1:n.717-151T>A
NM_000083.3:c.1167-151T>A MANE Select	NP_000074.3:n.1167-151T>A
NR_046453.2:n.1272-151T>A