Canonical Allele Identifier: CA369684126

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143018588T>A (hg19) ; chr7:g.143321495T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321495T>A , CM000669.2:g.143321495T>A	GRCh38
NC_000007.13:g.143018588T>A , CM000669.1:g.143018588T>A	GRCh37
NC_000007.12:g.142728710T>A	NCBI36
NG_009815.1:g.10370T>A
NG_009815.2:g.10370T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.562+2T>A	ENSP00000498052.2:n.562+2T>A
ENST00000343257.7:c.562+2T>A MANE Select	ENSP00000339867.2:n.562+2T>A
ENST00000432192.6:c.330+2T>A
ENST00000455478.6:c.16+2T>A	ENSP00000400027.2:n.16+2T>A
ENST00000650516.1:c.562+2T>A	ENSP00000498052.1:n.562+2T>A
ENST00000343257.6:c.562+2T>A	ENSP00000339867.2:n.562+2T>A
ENST00000432192.5:c.20+2T>A
ENST00000455478.5:c.20+2T>A
ENST00000495612.1:n.20+2T>A
NM_000083.2:c.562+2T>A	NP_000074.2:n.562+2T>A
NR_046453.1:n.649+2T>A
XM_011515781.1:c.562+2T>A	XP_011514083.1:n.562+2T>A
XM_017011739.1:c.269+2T>A	XP_016867228.1:n.269+2T>A
XM_017011740.1:c.269+2T>A	XP_016867229.1:n.269+2T>A
NM_000083.3:c.562+2T>A MANE Select	NP_000074.3:n.562+2T>A
NR_046453.2:n.664+2T>A