Canonical Allele Identifier: CA1748892844
Gene: CLCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143339448T= , CM000669.2:g.143339448T= GRCh38
NC_000007.13:g.143036541T= , CM000669.1:g.143036541T= GRCh37
NC_000007.12:g.142746663T= NCBI36
NG_009815.1:g.28323T=
NG_009815.2:g.28323T=

Transcript Alleles

HGVS Amino-acid change
ENST00000650516.2:c.1472-63T= ENSP00000498052.2:n.1472-63T=
ENST00000343257.7:c.1472-63T= MANE Select ENSP00000339867.2:n.1472-63T=
ENST00000432192.6:c.1296-63T=
ENST00000343257.6:c.1472-63T= ENSP00000339867.2:n.1472-63T=
NM_000083.2:c.1472-63T= NP_000074.2:n.1472-63T=
NR_046453.1:n.1412-63T=
XM_011515781.1:c.1496-63T= XP_011514083.1:n.1496-63T=
XM_011515782.1:c.218-63T= XP_011514084.1:n.218-63T=
XM_011515782.2:c.218-63T= XP_011514084.1:n.218-63T=
XM_017011739.1:c.1046-63T= XP_016867228.1:n.1046-63T=
XM_017011740.1:c.1022-63T= XP_016867229.1:n.1022-63T=
NM_000083.3:c.1472-63T= MANE Select NP_000074.3:n.1472-63T=
NR_046453.2:n.1427-63T=