Canonical Allele Identifier: CA369645302

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143036370A>G (hg19) ; chr7:g.143339277A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143339277A>G , CM000669.2:g.143339277A>G	GRCh38
NC_000007.13:g.143036370A>G , CM000669.1:g.143036370A>G	GRCh37
NC_000007.12:g.142746492A>G	NCBI36
NG_009815.1:g.28152A>G
NG_009815.2:g.28152A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1426A>G	ENSP00000498052.2:p.Thr476Ala
ENST00000343257.7:c.1426A>G MANE Select	ENSP00000339867.2:p.Thr476Ala
ENST00000432192.6:c.1250A>G
ENST00000343257.6:c.1426A>G	ENSP00000339867.2:p.Thr476Ala
NM_000083.2:c.1426A>G	NP_000074.2:p.Thr476Ala
NR_046453.1:n.1366A>G
XM_011515781.1:c.1450A>G	XP_011514083.1:p.Thr484Ala
XM_011515782.1:c.172A>G	XP_011514084.1:p.Thr58Ala
XM_011515782.2:c.172A>G	XP_011514084.1:p.Thr58Ala
XM_017011739.1:c.1000A>G	XP_016867228.1:p.Thr334Ala
XM_017011740.1:c.976A>G	XP_016867229.1:p.Thr326Ala
NM_000083.3:c.1426A>G MANE Select	NP_000074.3:p.Thr476Ala
NR_046453.2:n.1381A>G