Canonical Allele Identifier: CA1748881670
Gene: CLCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143321733T= , CM000669.2:g.143321733T= GRCh38
NC_000007.13:g.143018826T= , CM000669.1:g.143018826T= GRCh37
NC_000007.12:g.142728948T= NCBI36
NG_009815.1:g.10608T=
NG_009815.2:g.10608T=

Transcript Alleles

HGVS Amino-acid change
ENST00000650516.2:c.581T= ENSP00000498052.2:p.Met194=
ENST00000343257.7:c.581T= MANE Select ENSP00000339867.2:p.Met194=
ENST00000432192.6:c.349T=
ENST00000455478.6:c.35T= ENSP00000400027.2:p.Met12=
ENST00000650516.1:c.581T= ENSP00000498052.1:p.Met194=
ENST00000343257.6:c.581T= ENSP00000339867.2:p.Met194=
ENST00000432192.5:c.39T=
ENST00000455478.5:c.39T=
ENST00000495612.1:n.39T=
NM_000083.2:c.581T= NP_000074.2:p.Met194=
NR_046453.1:n.668T=
XM_011515781.1:c.581T= XP_011514083.1:p.Met194=
XM_017011739.1:c.288T= XP_016867228.1:p.Asn96=
XM_017011740.1:c.288T= XP_016867229.1:p.Asn96=
NM_000083.3:c.581T= MANE Select NP_000074.3:p.Met194=
NR_046453.2:n.683T=