Canonical Allele Identifier: CA369653666

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143048807A>G (hg19) ; chr7:g.143351714A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351714A>G , CM000669.2:g.143351714A>G	GRCh38
NC_000007.13:g.143048807A>G , CM000669.1:g.143048807A>G	GRCh37
NC_000007.12:g.142758929A>G	NCBI36
NG_009815.1:g.40589A>G
NG_009815.2:g.40589A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2716A>G	ENSP00000498052.2:p.Asn906Asp
ENST00000343257.7:c.2716A>G MANE Select	ENSP00000339867.2:p.Asn906Asp
ENST00000432192.6:c.2540A>G
ENST00000343257.6:c.2716A>G	ENSP00000339867.2:p.Asn906Asp
NM_000083.2:c.2716A>G	NP_000074.2:p.Asn906Asp
NR_046453.1:n.2656A>G
XM_011515781.1:c.2740A>G	XP_011514083.1:p.Asn914Asp
XM_011515782.1:c.1462A>G	XP_011514084.1:p.Asn488Asp
XM_011515782.2:c.1462A>G	XP_011514084.1:p.Asn488Asp
XM_017011739.1:c.2290A>G	XP_016867228.1:p.Asn764Asp
XM_017011740.1:c.2266A>G	XP_016867229.1:p.Asn756Asp
NM_000083.3:c.2716A>G MANE Select	NP_000074.3:p.Asn906Asp
NR_046453.2:n.2671A>G