Canonical Allele Identifier: CA369653432

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143048691A>C (hg19) ; chr7:g.143351598A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351598A>C , CM000669.2:g.143351598A>C	GRCh38
NC_000007.13:g.143048691A>C , CM000669.1:g.143048691A>C	GRCh37
NC_000007.12:g.142758813A>C	NCBI36
NG_009815.1:g.40473A>C
NG_009815.2:g.40473A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2600A>C	ENSP00000498052.2:p.Gln867Pro
ENST00000343257.7:c.2600A>C MANE Select	ENSP00000339867.2:p.Gln867Pro
ENST00000432192.6:c.2424A>C
ENST00000343257.6:c.2600A>C	ENSP00000339867.2:p.Gln867Pro
NM_000083.2:c.2600A>C	NP_000074.2:p.Gln867Pro
NR_046453.1:n.2540A>C
XM_011515781.1:c.2624A>C	XP_011514083.1:p.Gln875Pro
XM_011515782.1:c.1346A>C	XP_011514084.1:p.Gln449Pro
XM_011515782.2:c.1346A>C	XP_011514084.1:p.Gln449Pro
XM_017011739.1:c.2174A>C	XP_016867228.1:p.Gln725Pro
XM_017011740.1:c.2150A>C	XP_016867229.1:p.Gln717Pro
NM_000083.3:c.2600A>C MANE Select	NP_000074.3:p.Gln867Pro
NR_046453.2:n.2555A>C