Canonical Allele Identifier: CA369684316

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143018825A>C (hg19) ; chr7:g.143321732A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321732A>C , CM000669.2:g.143321732A>C	GRCh38
NC_000007.13:g.143018825A>C , CM000669.1:g.143018825A>C	GRCh37
NC_000007.12:g.142728947A>C	NCBI36
NG_009815.1:g.10607A>C
NG_009815.2:g.10607A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.580A>C	ENSP00000498052.2:p.Met194Leu
ENST00000343257.7:c.580A>C MANE Select	ENSP00000339867.2:p.Met194Leu
ENST00000432192.6:c.348A>C
ENST00000455478.6:c.34A>C	ENSP00000400027.2:p.Met12Leu
ENST00000650516.1:c.580A>C	ENSP00000498052.1:p.Met194Leu
ENST00000343257.6:c.580A>C	ENSP00000339867.2:p.Met194Leu
ENST00000432192.5:c.38A>C
ENST00000455478.5:c.38A>C
ENST00000495612.1:n.38A>C
NM_000083.2:c.580A>C	NP_000074.2:p.Met194Leu
NR_046453.1:n.667A>C
XM_011515781.1:c.580A>C	XP_011514083.1:p.Met194Leu
XM_017011739.1:c.287A>C	XP_016867228.1:p.Asn96Thr
XM_017011740.1:c.287A>C	XP_016867229.1:p.Asn96Thr
NM_000083.3:c.580A>C MANE Select	NP_000074.3:p.Met194Leu
NR_046453.2:n.682A>C