Canonical Allele Identifier: CA369684776

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143018886C>T (hg19) ; chr7:g.143321793C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321793C>T , CM000669.2:g.143321793C>T	GRCh38
NC_000007.13:g.143018886C>T , CM000669.1:g.143018886C>T	GRCh37
NC_000007.12:g.142729008C>T	NCBI36
NG_009815.1:g.10668C>T
NG_009815.2:g.10668C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.641C>T	ENSP00000498052.2:p.Ala214Val
ENST00000343257.7:c.641C>T MANE Select	ENSP00000339867.2:p.Ala214Val
ENST00000432192.6:c.409C>T
ENST00000455478.6:c.95C>T	ENSP00000400027.2:p.Ala32Val
ENST00000650516.1:c.641C>T	ENSP00000498052.1:p.Ala214Val
ENST00000343257.6:c.641C>T	ENSP00000339867.2:p.Ala214Val
ENST00000432192.5:c.99C>T
ENST00000455478.5:c.99C>T
ENST00000495612.1:n.99C>T
NM_000083.2:c.641C>T	NP_000074.2:p.Ala214Val
NR_046453.1:n.728C>T
XM_011515781.1:c.641C>T	XP_011514083.1:p.Ala214Val
XM_017011739.1:c.348C>T	XP_016867228.1:p.Gly116=
XM_017011740.1:c.348C>T	XP_016867229.1:p.Gly116=
NM_000083.3:c.641C>T MANE Select	NP_000074.3:p.Ala214Val
NR_046453.2:n.743C>T