Canonical Allele Identifier: CA369684699

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143018875A>C (hg19) ; chr7:g.143321782A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321782A>C , CM000669.2:g.143321782A>C	GRCh38
NC_000007.13:g.143018875A>C , CM000669.1:g.143018875A>C	GRCh37
NC_000007.12:g.142728997A>C	NCBI36
NG_009815.1:g.10657A>C
NG_009815.2:g.10657A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.630A>C	ENSP00000498052.2:p.Lys210Asn
ENST00000343257.7:c.630A>C MANE Select	ENSP00000339867.2:p.Lys210Asn
ENST00000432192.6:c.398A>C
ENST00000455478.6:c.84A>C	ENSP00000400027.2:p.Lys28Asn
ENST00000650516.1:c.630A>C	ENSP00000498052.1:p.Lys210Asn
ENST00000343257.6:c.630A>C	ENSP00000339867.2:p.Lys210Asn
ENST00000432192.5:c.88A>C
ENST00000455478.5:c.88A>C
ENST00000495612.1:n.88A>C
NM_000083.2:c.630A>C	NP_000074.2:p.Lys210Asn
NR_046453.1:n.717A>C
XM_011515781.1:c.630A>C	XP_011514083.1:p.Lys210Asn
XM_017011739.1:c.337A>C	XP_016867228.1:p.Ser113Arg
XM_017011740.1:c.337A>C	XP_016867229.1:p.Ser113Arg
NM_000083.3:c.630A>C MANE Select	NP_000074.3:p.Lys210Asn
NR_046453.2:n.732A>C