Canonical Allele Identifier: CA369654132

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143048988T>G (hg19) ; chr7:g.143351895T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351895T>G , CM000669.2:g.143351895T>G	GRCh38
NC_000007.13:g.143048988T>G , CM000669.1:g.143048988T>G	GRCh37
NC_000007.12:g.142759110T>G	NCBI36
NG_009815.1:g.40770T>G
NG_009815.2:g.40770T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2897T>G	ENSP00000498052.2:p.Leu966Arg
ENST00000343257.7:c.2897T>G MANE Select	ENSP00000339867.2:p.Leu966Arg
ENST00000343257.6:c.2897T>G	ENSP00000339867.2:p.Leu966Arg
NM_000083.2:c.2897T>G	NP_000074.2:p.Leu966Arg
NR_046453.1:n.2837T>G
XM_011515781.1:c.2921T>G	XP_011514083.1:p.Leu974Arg
XM_011515782.1:c.1643T>G	XP_011514084.1:p.Leu548Arg
XM_011515782.2:c.1643T>G	XP_011514084.1:p.Leu548Arg
XM_017011739.1:c.2471T>G	XP_016867228.1:p.Leu824Arg
XM_017011740.1:c.2447T>G	XP_016867229.1:p.Leu816Arg
NM_000083.3:c.2897T>G MANE Select	NP_000074.3:p.Leu966Arg
NR_046453.2:n.2852T>G