Canonical Allele Identifier: CA369687561

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143021553G>T (hg19) ; chr7:g.143324460G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143324460G>T , CM000669.2:g.143324460G>T	GRCh38
NC_000007.13:g.143021553G>T , CM000669.1:g.143021553G>T	GRCh37
NC_000007.12:g.142731675G>T	NCBI36
NG_009815.1:g.13335G>T
NG_009815.2:g.13335G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.853+563G>T	ENSP00000498052.2:n.853+563G>T
ENST00000343257.7:c.821G>T MANE Select	ENSP00000339867.2:p.Gly274Val
ENST00000432192.6:c.645G>T
ENST00000455478.6:c.409G>T	ENSP00000400027.2:n.409G>T
ENST00000650516.1:c.853+563G>T	ENSP00000498052.1:n.853+563G>T
ENST00000343257.6:c.821G>T	ENSP00000339867.2:p.Gly274Val
ENST00000432192.5:c.335G>T
ENST00000455478.5:c.413G>T
ENST00000495612.1:n.154+2612G>T
NM_000083.2:c.821G>T	NP_000074.2:p.Gly274Val
NR_046453.1:n.911G>T
XM_011515781.1:c.853+563G>T	XP_011514083.1:n.853+563G>T
XM_017011739.1:c.403+2612G>T	XP_016867228.1:n.403+2612G>T
XM_017011740.1:c.403+2612G>T	XP_016867229.1:n.403+2612G>T
NM_000083.3:c.821G>T MANE Select	NP_000074.3:p.Gly274Val
NR_046453.2:n.926G>T