Canonical Allele Identifier: CA168255315

Gene: CLCN1

Linked Data

• dbSNP Id: rs765459509
• MyVariant Identifiers: chr7:g.143018374A>C (hg19) ; chr7:g.143321281A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321281A>C , CM000669.2:g.143321281A>C	GRCh38
NC_000007.13:g.143018374A>C , CM000669.1:g.143018374A>C	GRCh37
NC_000007.12:g.142728496A>C	NCBI36
NG_009815.1:g.10156A>C
NG_009815.2:g.10156A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.434-84A>C	ENSP00000498052.2:n.434-84A>C
ENST00000343257.7:c.434-84A>C MANE Select	ENSP00000339867.2:n.434-84A>C
ENST00000432192.6:c.202-84A>C
ENST00000650516.1:c.434-84A>C	ENSP00000498052.1:n.434-84A>C
ENST00000343257.6:c.434-84A>C	ENSP00000339867.2:n.434-84A>C
NM_000083.2:c.434-84A>C	NP_000074.2:n.434-84A>C
NR_046453.1:n.521-84A>C
XM_011515781.1:c.434-84A>C	XP_011514083.1:n.434-84A>C
XM_017011739.1:c.141-84A>C	XP_016867228.1:n.141-84A>C
XM_017011740.1:c.141-84A>C	XP_016867229.1:n.141-84A>C
NM_000083.3:c.434-84A>C MANE Select	NP_000074.3:n.434-84A>C
NR_046453.2:n.536-84A>C