Canonical Allele Identifier: CA1748881697
Gene: CLCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143321744C= , CM000669.2:g.143321744C= GRCh38
NC_000007.13:g.143018837C= , CM000669.1:g.143018837C= GRCh37
NC_000007.12:g.142728959C= NCBI36
NG_009815.1:g.10619C=
NG_009815.2:g.10619C=

Transcript Alleles

HGVS Amino-acid change
ENST00000650516.2:c.592C= ENSP00000498052.2:p.Leu198=
ENST00000343257.7:c.592C= MANE Select ENSP00000339867.2:p.Leu198=
ENST00000432192.6:c.360C=
ENST00000455478.6:c.46C= ENSP00000400027.2:p.Leu16=
ENST00000650516.1:c.592C= ENSP00000498052.1:p.Leu198=
ENST00000343257.6:c.592C= ENSP00000339867.2:p.Leu198=
ENST00000432192.5:c.50C=
ENST00000455478.5:c.50C=
ENST00000495612.1:n.50C=
NM_000083.2:c.592C= NP_000074.2:p.Leu198=
NR_046453.1:n.679C=
XM_011515781.1:c.592C= XP_011514083.1:p.Leu198=
XM_017011739.1:c.299C= XP_016867228.1:p.Thr100=
XM_017011740.1:c.299C= XP_016867229.1:p.Thr100=
NM_000083.3:c.592C= MANE Select NP_000074.3:p.Leu198=
NR_046453.2:n.694C=