Canonical Allele Identifier: CA4536909

Gene: CLCN1

Linked Data

• ClinVar Variation Id: 462843
• ClinVar RCV Id: RCV000559881 ; RCV000612704 ; RCV001161534
• dbSNP Id: rs113839156
• ExAC: 7:143017753 C / T
• gnomAD v2: 7-143017753-C-T
• gnomAD v3: 7-143320660-C-T
• gnomAD v4: 7-143320660-C-T
• MyVariant Identifiers: chr7:g.143017753C>T (hg19) ; chr7:g.143320660C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143320660C>T , CM000669.2:g.143320660C>T	GRCh38
NC_000007.13:g.143017753C>T , CM000669.1:g.143017753C>T	GRCh37
NC_000007.12:g.142727875C>T	NCBI36
NG_009815.1:g.9535C>T
NG_009815.2:g.9535C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.302-4C>T	ENSP00000498052.2:n.302-4C>T
ENST00000343257.7:c.302-4C>T MANE Select	ENSP00000339867.2:n.302-4C>T
ENST00000432192.6:c.70-4C>T
ENST00000650516.1:c.302-4C>T	ENSP00000498052.1:n.302-4C>T
ENST00000343257.6:c.302-4C>T	ENSP00000339867.2:n.302-4C>T
NM_000083.2:c.302-4C>T	NP_000074.2:n.302-4C>T
NR_046453.1:n.389-4C>T
XM_011515781.1:c.302-4C>T	XP_011514083.1:n.302-4C>T
XM_017011739.1:c.9-4C>T	XP_016867228.1:n.9-4C>T
XM_017011740.1:c.9-4C>T	XP_016867229.1:n.9-4C>T
NM_000083.3:c.302-4C>T MANE Select	NP_000074.3:n.302-4C>T
NR_046453.2:n.404-4C>T