Canonical Allele Identifier: CA1748892888
Gene: CLCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143339549A= , CM000669.2:g.143339549A= GRCh38
NC_000007.13:g.143036642A= , CM000669.1:g.143036642A= GRCh37
NC_000007.12:g.142746764A= NCBI36
NG_009815.1:g.28424A=
NG_009815.2:g.28424A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000650516.2:c.1510A= ENSP00000498052.2:p.Met504=
ENST00000343257.7:c.1510A= MANE Select ENSP00000339867.2:p.Met504=
ENST00000432192.6:c.1334A=
ENST00000343257.6:c.1510A= ENSP00000339867.2:p.Met504=
NM_000083.2:c.1510A= NP_000074.2:p.Met504=
NR_046453.1:n.1450A=
XM_011515781.1:c.1534A= XP_011514083.1:p.Met512=
XM_011515782.1:c.256A= XP_011514084.1:p.Met86=
XM_011515782.2:c.256A= XP_011514084.1:p.Met86=
XM_017011739.1:c.1084A= XP_016867228.1:p.Met362=
XM_017011740.1:c.1060A= XP_016867229.1:p.Met354=
NM_000083.3:c.1510A= MANE Select NP_000074.3:p.Met504=
NR_046453.2:n.1465A=