Canonical Allele Identifier: CA458542320
Gene: CLCN1 HGNC NCBI

Linked Data

COSMIC: COSM745182
MyVariant Identifiers: chr7:g.143048731C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143351638C>T , CM000669.2:g.143351638C>T GRCh38
NC_000007.13:g.143048731C>T , CM000669.1:g.143048731C>T GRCh37
NC_000007.12:g.142758853C>T NCBI36
NG_009815.1:g.40513C>T
NG_009815.2:g.40513C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000650516.2:c.2640C>T ENSP00000498052.2:p.Leu880=
ENST00000343257.7:c.2640C>T MANE Select ENSP00000339867.2:p.Leu880=
ENST00000432192.6:c.2464C>T
ENST00000343257.6:c.2640C>T ENSP00000339867.2:p.Leu880=
NM_000083.2:c.2640C>T NP_000074.2:p.Leu880=
NR_046453.1:n.2580C>T
XM_011515781.1:c.2664C>T XP_011514083.1:p.Leu888=
XM_011515782.1:c.1386C>T XP_011514084.1:p.Leu462=
XM_011515782.2:c.1386C>T XP_011514084.1:p.Leu462=
XM_017011739.1:c.2214C>T XP_016867228.1:p.Leu738=
XM_017011740.1:c.2190C>T XP_016867229.1:p.Leu730=
NM_000083.3:c.2640C>T MANE Select NP_000074.3:p.Leu880=
NR_046453.2:n.2595C>T