Canonical Allele Identifier: CA369654123

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143048986G>T (hg19) ; chr7:g.143351893G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351893G>T , CM000669.2:g.143351893G>T	GRCh38
NC_000007.13:g.143048986G>T , CM000669.1:g.143048986G>T	GRCh37
NC_000007.12:g.142759108G>T	NCBI36
NG_009815.1:g.40768G>T
NG_009815.2:g.40768G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2895G>T	ENSP00000498052.2:p.Glu965Asp
ENST00000343257.7:c.2895G>T MANE Select	ENSP00000339867.2:p.Glu965Asp
ENST00000343257.6:c.2895G>T	ENSP00000339867.2:p.Glu965Asp
NM_000083.2:c.2895G>T	NP_000074.2:p.Glu965Asp
NR_046453.1:n.2835G>T
XM_011515781.1:c.2919G>T	XP_011514083.1:p.Glu973Asp
XM_011515782.1:c.1641G>T	XP_011514084.1:p.Glu547Asp
XM_011515782.2:c.1641G>T	XP_011514084.1:p.Glu547Asp
XM_017011739.1:c.2469G>T	XP_016867228.1:p.Glu823Asp
XM_017011740.1:c.2445G>T	XP_016867229.1:p.Glu815Asp
NM_000083.3:c.2895G>T MANE Select	NP_000074.3:p.Glu965Asp
NR_046453.2:n.2850G>T