Canonical Allele Identifier: CA369653789

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143048867T>G (hg19) ; chr7:g.143351774T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351774T>G , CM000669.2:g.143351774T>G	GRCh38
NC_000007.13:g.143048867T>G , CM000669.1:g.143048867T>G	GRCh37
NC_000007.12:g.142758989T>G	NCBI36
NG_009815.1:g.40649T>G
NG_009815.2:g.40649T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2776T>G	ENSP00000498052.2:p.Ser926Ala
ENST00000343257.7:c.2776T>G MANE Select	ENSP00000339867.2:p.Ser926Ala
ENST00000343257.6:c.2776T>G	ENSP00000339867.2:p.Ser926Ala
NM_000083.2:c.2776T>G	NP_000074.2:p.Ser926Ala
NR_046453.1:n.2716T>G
XM_011515781.1:c.2800T>G	XP_011514083.1:p.Ser934Ala
XM_011515782.1:c.1522T>G	XP_011514084.1:p.Ser508Ala
XM_011515782.2:c.1522T>G	XP_011514084.1:p.Ser508Ala
XM_017011739.1:c.2350T>G	XP_016867228.1:p.Ser784Ala
XM_017011740.1:c.2326T>G	XP_016867229.1:p.Ser776Ala
NM_000083.3:c.2776T>G MANE Select	NP_000074.3:p.Ser926Ala
NR_046453.2:n.2731T>G