Canonical Allele Identifier: CA369684033

Gene: CLCN1

Linked Data

• dbSNP Id: rs1802431832
• MyVariant Identifiers: chr7:g.143018574C>A (hg19) ; chr7:g.143321481C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321481C>A , CM000669.2:g.143321481C>A	GRCh38
NC_000007.13:g.143018574C>A , CM000669.1:g.143018574C>A	GRCh37
NC_000007.12:g.142728696C>A	NCBI36
NG_009815.1:g.10356C>A
NG_009815.2:g.10356C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.550C>A	ENSP00000498052.2:p.Pro184Thr
ENST00000343257.7:c.550C>A MANE Select	ENSP00000339867.2:p.Pro184Thr
ENST00000432192.6:c.318C>A
ENST00000455478.6:c.4C>A	ENSP00000400027.2:p.Pro2Thr
ENST00000650516.1:c.550C>A	ENSP00000498052.1:p.Pro184Thr
ENST00000343257.6:c.550C>A	ENSP00000339867.2:p.Pro184Thr
ENST00000432192.5:c.8C>A
ENST00000455478.5:c.8C>A
ENST00000495612.1:n.8C>A
NM_000083.2:c.550C>A	NP_000074.2:p.Pro184Thr
NR_046453.1:n.637C>A
XM_011515781.1:c.550C>A	XP_011514083.1:p.Pro184Thr
XM_017011739.1:c.257C>A	XP_016867228.1:p.Ser86Tyr
XM_017011740.1:c.257C>A	XP_016867229.1:p.Ser86Tyr
NM_000083.3:c.550C>A MANE Select	NP_000074.3:p.Pro184Thr
NR_046453.2:n.652C>A