Canonical Allele Identifier: CA458283210

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143039029A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143341936A>T , CM000669.2:g.143341936A>T	GRCh38
NC_000007.13:g.143039029A>T , CM000669.1:g.143039029A>T	GRCh37
NC_000007.12:g.142749151A>T	NCBI36
NG_009815.1:g.30811A>T
NG_009815.2:g.30811A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.1590A>T	ENSP00000498052.2:p.Ala530=
ENST00000343257.7:c.1590A>T MANE Select	ENSP00000339867.2:p.Ala530=
ENST00000432192.6:c.1414A>T
ENST00000343257.6:c.1590A>T	ENSP00000339867.2:p.Ala530=
NM_000083.2:c.1590A>T	NP_000074.2:p.Ala530=
NR_046453.1:n.1530A>T
XM_011515781.1:c.1614A>T	XP_011514083.1:p.Ala538=
XM_011515782.1:c.336A>T	XP_011514084.1:p.Ala112=
XM_011515782.2:c.336A>T	XP_011514084.1:p.Ala112=
XM_017011739.1:c.1164A>T	XP_016867228.1:p.Ala388=
XM_017011740.1:c.1140A>T	XP_016867229.1:p.Ala380=
NM_000083.3:c.1590A>T MANE Select	NP_000074.3:p.Ala530=
NR_046453.2:n.1545A>T