Canonical Allele Identifier: CA369653664

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143048806G>T (hg19) ; chr7:g.143351713G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351713G>T , CM000669.2:g.143351713G>T	GRCh38
NC_000007.13:g.143048806G>T , CM000669.1:g.143048806G>T	GRCh37
NC_000007.12:g.142758928G>T	NCBI36
NG_009815.1:g.40588G>T
NG_009815.2:g.40588G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2715G>T	ENSP00000498052.2:p.Glu905Asp
ENST00000343257.7:c.2715G>T MANE Select	ENSP00000339867.2:p.Glu905Asp
ENST00000432192.6:c.2539G>T
ENST00000343257.6:c.2715G>T	ENSP00000339867.2:p.Glu905Asp
NM_000083.2:c.2715G>T	NP_000074.2:p.Glu905Asp
NR_046453.1:n.2655G>T
XM_011515781.1:c.2739G>T	XP_011514083.1:p.Glu913Asp
XM_011515782.1:c.1461G>T	XP_011514084.1:p.Glu487Asp
XM_011515782.2:c.1461G>T	XP_011514084.1:p.Glu487Asp
XM_017011739.1:c.2289G>T	XP_016867228.1:p.Glu763Asp
XM_017011740.1:c.2265G>T	XP_016867229.1:p.Glu755Asp
NM_000083.3:c.2715G>T MANE Select	NP_000074.3:p.Glu905Asp
NR_046453.2:n.2670G>T