Canonical Allele Identifier: CA369654029

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143048963G>C (hg19) ; chr7:g.143351870G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351870G>C , CM000669.2:g.143351870G>C	GRCh38
NC_000007.13:g.143048963G>C , CM000669.1:g.143048963G>C	GRCh37
NC_000007.12:g.142759085G>C	NCBI36
NG_009815.1:g.40745G>C
NG_009815.2:g.40745G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2872G>C	ENSP00000498052.2:p.Glu958Gln
ENST00000343257.7:c.2872G>C MANE Select	ENSP00000339867.2:p.Glu958Gln
ENST00000343257.6:c.2872G>C	ENSP00000339867.2:p.Glu958Gln
NM_000083.2:c.2872G>C	NP_000074.2:p.Glu958Gln
NR_046453.1:n.2812G>C
XM_011515781.1:c.2896G>C	XP_011514083.1:p.Glu966Gln
XM_011515782.1:c.1618G>C	XP_011514084.1:p.Glu540Gln
XM_011515782.2:c.1618G>C	XP_011514084.1:p.Glu540Gln
XM_017011739.1:c.2446G>C	XP_016867228.1:p.Glu816Gln
XM_017011740.1:c.2422G>C	XP_016867229.1:p.Glu808Gln
NM_000083.3:c.2872G>C MANE Select	NP_000074.3:p.Glu958Gln
NR_046453.2:n.2827G>C