Canonical Allele Identifier: CA369646695

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143039188G>C (hg19) ; chr7:g.143342095G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143342095G>C , CM000669.2:g.143342095G>C	GRCh38
NC_000007.13:g.143039188G>C , CM000669.1:g.143039188G>C	GRCh37
NC_000007.12:g.142749310G>C	NCBI36
NG_009815.1:g.30970G>C
NG_009815.2:g.30970G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1749G>C	ENSP00000498052.2:p.Gln583His
ENST00000343257.7:c.1749G>C MANE Select	ENSP00000339867.2:p.Gln583His
ENST00000432192.6:c.1573G>C
ENST00000343257.6:c.1749G>C	ENSP00000339867.2:p.Gln583His
NM_000083.2:c.1749G>C	NP_000074.2:p.Gln583His
NR_046453.1:n.1689G>C
XM_011515781.1:c.1773G>C	XP_011514083.1:p.Gln591His
XM_011515782.1:c.495G>C	XP_011514084.1:p.Gln165His
XM_011515782.2:c.495G>C	XP_011514084.1:p.Gln165His
XM_017011739.1:c.1323G>C	XP_016867228.1:p.Gln441His
XM_017011740.1:c.1299G>C	XP_016867229.1:p.Gln433His
NM_000083.3:c.1749G>C MANE Select	NP_000074.3:p.Gln583His
NR_046453.2:n.1704G>C