Canonical Allele Identifier: CA369683845

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143018545T>C (hg19) ; chr7:g.143321452T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321452T>C , CM000669.2:g.143321452T>C	GRCh38
NC_000007.13:g.143018545T>C , CM000669.1:g.143018545T>C	GRCh37
NC_000007.12:g.142728667T>C	NCBI36
NG_009815.1:g.10327T>C
NG_009815.2:g.10327T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.521T>C	ENSP00000498052.2:p.Phe174Ser
ENST00000343257.7:c.521T>C MANE Select	ENSP00000339867.2:p.Phe174Ser
ENST00000432192.6:c.289T>C
ENST00000650516.1:c.521T>C	ENSP00000498052.1:p.Phe174Ser
ENST00000343257.6:c.521T>C	ENSP00000339867.2:p.Phe174Ser
NM_000083.2:c.521T>C	NP_000074.2:p.Phe174Ser
NR_046453.1:n.608T>C
XM_011515781.1:c.521T>C	XP_011514083.1:p.Phe174Ser
XM_017011739.1:c.228T>C	XP_016867228.1:p.Leu76=
XM_017011740.1:c.228T>C	XP_016867229.1:p.Leu76=
NM_000083.3:c.521T>C MANE Select	NP_000074.3:p.Phe174Ser
NR_046453.2:n.623T>C