Canonical Allele Identifier: CA458280518

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143027866A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143330773A>T , CM000669.2:g.143330773A>T	GRCh38
NC_000007.13:g.143027866A>T , CM000669.1:g.143027866A>T	GRCh37
NC_000007.12:g.142737988A>T	NCBI36
NG_009815.1:g.19648A>T
NG_009815.2:g.19648A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.855A>T	ENSP00000498052.2:p.Gly285=
ENST00000343257.7:c.855A>T MANE Select	ENSP00000339867.2:p.Gly285=
ENST00000432192.6:c.679A>T
ENST00000455478.6:c.443A>T	ENSP00000400027.2:n.443A>T
ENST00000650516.1:c.855A>T	ENSP00000498052.1:p.Gly285=
ENST00000343257.6:c.855A>T	ENSP00000339867.2:p.Gly285=
ENST00000432192.5:c.369A>T
ENST00000455478.5:c.447A>T
ENST00000495612.1:n.156A>T
NM_000083.2:c.855A>T	NP_000074.2:p.Gly285=
NR_046453.1:n.945A>T
XM_011515781.1:c.855A>T	XP_011514083.1:p.Gly285=
XM_017011739.1:c.405A>T	XP_016867228.1:p.Gly135=
XM_017011740.1:c.405A>T	XP_016867229.1:p.Gly135=
NM_000083.3:c.855A>T MANE Select	NP_000074.3:p.Gly285=
NR_046453.2:n.960A>T