Canonical Allele Identifier: CA369646487

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143039093C>A (hg19) ; chr7:g.143342000C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143342000C>A , CM000669.2:g.143342000C>A	GRCh38
NC_000007.13:g.143039093C>A , CM000669.1:g.143039093C>A	GRCh37
NC_000007.12:g.142749215C>A	NCBI36
NG_009815.1:g.30875C>A
NG_009815.2:g.30875C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1654C>A	ENSP00000498052.2:p.Gln552Lys
ENST00000343257.7:c.1654C>A MANE Select	ENSP00000339867.2:p.Gln552Lys
ENST00000432192.6:c.1478C>A
ENST00000343257.6:c.1654C>A	ENSP00000339867.2:p.Gln552Lys
NM_000083.2:c.1654C>A	NP_000074.2:p.Gln552Lys
NR_046453.1:n.1594C>A
XM_011515781.1:c.1678C>A	XP_011514083.1:p.Gln560Lys
XM_011515782.1:c.400C>A	XP_011514084.1:p.Gln134Lys
XM_011515782.2:c.400C>A	XP_011514084.1:p.Gln134Lys
XM_017011739.1:c.1228C>A	XP_016867228.1:p.Gln410Lys
XM_017011740.1:c.1204C>A	XP_016867229.1:p.Gln402Lys
NM_000083.3:c.1654C>A MANE Select	NP_000074.3:p.Gln552Lys
NR_046453.2:n.1609C>A