Canonical Allele Identifier: CA369652607

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143350435C>T , CM000669.2:g.143350435C>T	GRCh38
NC_000007.13:g.143047528C>T , CM000669.1:g.143047528C>T	GRCh37
NC_000007.12:g.142757650C>T	NCBI36
NG_009815.1:g.39310C>T
NG_009815.2:g.39310C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000083.3:c.2467C>T MANE Select	NP_000074.3:p.Gln823Ter
ENST00000343257.7:c.2467C>T MANE Select	ENSP00000339867.2:p.Gln823Ter
NM_000083.2:c.2467C>T	NP_000074.2:p.Gln823Ter
NR_046453.1:n.2407C>T
NR_046453.2:n.2422C>T
ENST00000343257.6:c.2467C>T	ENSP00000339867.2:p.Gln823Ter
ENST00000432192.6:c.2291C>T
ENST00000650516.2:c.2467C>T	ENSP00000498052.2:p.Gln823Ter
XM_011515781.1:c.2491C>T	XP_011514083.1:p.Gln831Ter
XM_011515782.1:c.1213C>T	XP_011514084.1:p.Gln405Ter
XM_011515782.2:c.1213C>T	XP_011514084.1:p.Gln405Ter
XM_017011739.1:c.2041C>T	XP_016867228.1:p.Gln681Ter
XM_017011740.1:c.2017C>T	XP_016867229.1:p.Gln673Ter