Canonical Allele Identifier: CA458542611

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143049010C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351917C>G , CM000669.2:g.143351917C>G	GRCh38
NC_000007.13:g.143049010C>G , CM000669.1:g.143049010C>G	GRCh37
NC_000007.12:g.142759132C>G	NCBI36
NG_009815.1:g.40792C>G
NG_009815.2:g.40792C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2919C>G	ENSP00000498052.2:p.Pro973=
ENST00000343257.7:c.2919C>G MANE Select	ENSP00000339867.2:p.Pro973=
ENST00000343257.6:c.2919C>G	ENSP00000339867.2:p.Pro973=
NM_000083.2:c.2919C>G	NP_000074.2:p.Pro973=
NR_046453.1:n.2859C>G
XM_011515781.1:c.2943C>G	XP_011514083.1:p.Pro981=
XM_011515782.1:c.1665C>G	XP_011514084.1:p.Pro555=
XM_011515782.2:c.1665C>G	XP_011514084.1:p.Pro555=
XM_017011739.1:c.2493C>G	XP_016867228.1:p.Pro831=
XM_017011740.1:c.2469C>G	XP_016867229.1:p.Pro823=
NM_000083.3:c.2919C>G MANE Select	NP_000074.3:p.Pro973=
NR_046453.2:n.2874C>G