Canonical Allele Identifier: CA369645629

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143036632A>C (hg19) ; chr7:g.143339539A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143339539A>C , CM000669.2:g.143339539A>C	GRCh38
NC_000007.13:g.143036632A>C , CM000669.1:g.143036632A>C	GRCh37
NC_000007.12:g.142746754A>C	NCBI36
NG_009815.1:g.28414A>C
NG_009815.2:g.28414A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.1500A>C	ENSP00000498052.2:p.Glu500Asp
ENST00000343257.7:c.1500A>C MANE Select	ENSP00000339867.2:p.Glu500Asp
ENST00000432192.6:c.1324A>C
ENST00000343257.6:c.1500A>C	ENSP00000339867.2:p.Glu500Asp
NM_000083.2:c.1500A>C	NP_000074.2:p.Glu500Asp
NR_046453.1:n.1440A>C
XM_011515781.1:c.1524A>C	XP_011514083.1:p.Glu508Asp
XM_011515782.1:c.246A>C	XP_011514084.1:p.Glu82Asp
XM_011515782.2:c.246A>C	XP_011514084.1:p.Glu82Asp
XM_017011739.1:c.1074A>C	XP_016867228.1:p.Glu358Asp
XM_017011740.1:c.1050A>C	XP_016867229.1:p.Glu350Asp
NM_000083.3:c.1500A>C MANE Select	NP_000074.3:p.Glu500Asp
NR_046453.2:n.1455A>C