Canonical Allele Identifier: CA369653650

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143048799C>A (hg19) ; chr7:g.143351706C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351706C>A , CM000669.2:g.143351706C>A	GRCh38
NC_000007.13:g.143048799C>A , CM000669.1:g.143048799C>A	GRCh37
NC_000007.12:g.142758921C>A	NCBI36
NG_009815.1:g.40581C>A
NG_009815.2:g.40581C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2708C>A	ENSP00000498052.2:p.Ser903Tyr
ENST00000343257.7:c.2708C>A MANE Select	ENSP00000339867.2:p.Ser903Tyr
ENST00000432192.6:c.2532C>A
ENST00000343257.6:c.2708C>A	ENSP00000339867.2:p.Ser903Tyr
NM_000083.2:c.2708C>A	NP_000074.2:p.Ser903Tyr
NR_046453.1:n.2648C>A
XM_011515781.1:c.2732C>A	XP_011514083.1:p.Ser911Tyr
XM_011515782.1:c.1454C>A	XP_011514084.1:p.Ser485Tyr
XM_011515782.2:c.1454C>A	XP_011514084.1:p.Ser485Tyr
XM_017011739.1:c.2282C>A	XP_016867228.1:p.Ser761Tyr
XM_017011740.1:c.2258C>A	XP_016867229.1:p.Ser753Tyr
NM_000083.3:c.2708C>A MANE Select	NP_000074.3:p.Ser903Tyr
NR_046453.2:n.2663C>A