Canonical Allele Identifier: CA2579050559

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321693C>G , CM000669.2:g.143321693C>G	GRCh38
NC_000007.13:g.143018786C>G , CM000669.1:g.143018786C>G	GRCh37
NC_000007.12:g.142728908C>G	NCBI36
NG_009815.1:g.10568C>G
NG_009815.2:g.10568C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.563-22C>G	ENSP00000498052.2:n.563-22C>G
ENST00000343257.7:c.563-22C>G MANE Select	ENSP00000339867.2:n.563-22C>G
ENST00000432192.6:c.331-22C>G
ENST00000455478.6:c.17-22C>G	ENSP00000400027.2:n.17-22C>G
ENST00000650516.1:c.563-22C>G	ENSP00000498052.1:n.563-22C>G
ENST00000343257.6:c.563-22C>G	ENSP00000339867.2:n.563-22C>G
ENST00000432192.5:c.21-22C>G
ENST00000455478.5:c.21-22C>G
ENST00000495612.1:n.21-22C>G
NM_000083.2:c.563-22C>G	NP_000074.2:n.563-22C>G
NR_046453.1:n.650-22C>G
XM_011515781.1:c.563-22C>G	XP_011514083.1:n.563-22C>G
XM_017011739.1:c.270-22C>G	XP_016867228.1:n.270-22C>G
XM_017011740.1:c.270-22C>G	XP_016867229.1:n.270-22C>G
NM_000083.3:c.563-22C>G MANE Select	NP_000074.3:n.563-22C>G
NR_046453.2:n.665-22C>G