Canonical Allele Identifier: CA1748893874
Gene: CLCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143341840A= , CM000669.2:g.143341840A= GRCh38
NC_000007.13:g.143038933A= , CM000669.1:g.143038933A= GRCh37
NC_000007.12:g.142749055A= NCBI36
NG_009815.1:g.30715A=
NG_009815.2:g.30715A=

Transcript Alleles

HGVS Amino-acid change
ENST00000650516.2:c.1583-89A= ENSP00000498052.2:n.1583-89A=
ENST00000343257.7:c.1583-89A= MANE Select ENSP00000339867.2:n.1583-89A=
ENST00000432192.6:c.1407-89A=
ENST00000343257.6:c.1583-89A= ENSP00000339867.2:n.1583-89A=
NM_000083.2:c.1583-89A= NP_000074.2:n.1583-89A=
NR_046453.1:n.1523-89A=
XM_011515781.1:c.1607-89A= XP_011514083.1:n.1607-89A=
XM_011515782.1:c.329-89A= XP_011514084.1:n.329-89A=
XM_011515782.2:c.329-89A= XP_011514084.1:n.329-89A=
XM_017011739.1:c.1157-89A= XP_016867228.1:n.1157-89A=
XM_017011740.1:c.1133-89A= XP_016867229.1:n.1133-89A=
NM_000083.3:c.1583-89A= MANE Select NP_000074.3:n.1583-89A=
NR_046453.2:n.1538-89A=