Canonical Allele Identifier: CA369646847

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143039236G>T (hg19) ; chr7:g.143342143G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143342143G>T , CM000669.2:g.143342143G>T	GRCh38
NC_000007.13:g.143039236G>T , CM000669.1:g.143039236G>T	GRCh37
NC_000007.12:g.142749358G>T	NCBI36
NG_009815.1:g.31018G>T
NG_009815.2:g.31018G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1796+1G>T	ENSP00000498052.2:n.1796+1G>T
ENST00000343257.7:c.1796+1G>T MANE Select	ENSP00000339867.2:n.1796+1G>T
ENST00000432192.6:c.1620+1G>T
ENST00000343257.6:c.1796+1G>T	ENSP00000339867.2:n.1796+1G>T
NM_000083.2:c.1796+1G>T	NP_000074.2:n.1796+1G>T
NR_046453.1:n.1736+1G>T
XM_011515781.1:c.1820+1G>T	XP_011514083.1:n.1820+1G>T
XM_011515782.1:c.542+1G>T	XP_011514084.1:n.542+1G>T
XM_011515782.2:c.542+1G>T	XP_011514084.1:n.542+1G>T
XM_017011739.1:c.1370+1G>T	XP_016867228.1:n.1370+1G>T
XM_017011740.1:c.1346+1G>T	XP_016867229.1:n.1346+1G>T
NM_000083.3:c.1796+1G>T MANE Select	NP_000074.3:n.1796+1G>T
NR_046453.2:n.1751+1G>T