Canonical Allele Identifier: CA168214578

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143332871A>G , CM000669.2:g.143332871A>G	GRCh38
NC_000007.13:g.143029964A>G , CM000669.1:g.143029964A>G	GRCh37
NC_000007.12:g.142740086A>G	NCBI36
NG_009815.1:g.21746A>G
NG_009815.2:g.21746A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000083.3:c.1399A>G MANE Select	NP_000074.3:p.Lys467Glu
ENST00000343257.7:c.1399A>G MANE Select	ENSP00000339867.2:p.Lys467Glu
NM_000083.2:c.1399A>G	NP_000074.2:p.Lys467Glu
NR_046453.1:n.1341+368A>G
NR_046453.2:n.1356+368A>G
ENST00000343257.6:c.1399A>G	ENSP00000339867.2:p.Lys467Glu
ENST00000432192.6:c.1223A>G
ENST00000650516.2:c.1399A>G	ENSP00000498052.2:p.Lys467Glu
XM_011515781.1:c.1423A>G	XP_011514083.1:p.Lys475Glu
XM_011515782.1:c.145A>G	XP_011514084.1:p.Lys49Glu
XM_011515782.2:c.145A>G	XP_011514084.1:p.Lys49Glu
XM_017011739.1:c.973A>G	XP_016867228.1:p.Lys325Glu
XM_017011740.1:c.949A>G	XP_016867229.1:p.Lys317Glu