Canonical Allele Identifier: CA369683630

Gene: CLCN1

Linked Data

• ClinVar Variation Id: 2925419
• ClinVar RCV Id: RCV003781073
• dbSNP Id: rs1802429044
• MyVariant Identifiers: chr7:g.143018514T>C (hg19) ; chr7:g.143321421T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321421T>C , CM000669.2:g.143321421T>C	GRCh38
NC_000007.13:g.143018514T>C , CM000669.1:g.143018514T>C	GRCh37
NC_000007.12:g.142728636T>C	NCBI36
NG_009815.1:g.10296T>C
NG_009815.2:g.10296T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.490T>C	ENSP00000498052.2:p.Trp164Arg
ENST00000343257.7:c.490T>C MANE Select	ENSP00000339867.2:p.Trp164Arg
ENST00000432192.6:c.258T>C
ENST00000650516.1:c.490T>C	ENSP00000498052.1:p.Trp164Arg
ENST00000343257.6:c.490T>C	ENSP00000339867.2:p.Trp164Arg
NM_000083.2:c.490T>C	NP_000074.2:p.Trp164Arg
NR_046453.1:n.577T>C
XM_011515781.1:c.490T>C	XP_011514083.1:p.Trp164Arg
XM_017011739.1:c.197T>C	XP_016867228.1:p.Leu66Pro
XM_017011740.1:c.197T>C	XP_016867229.1:p.Leu66Pro
NM_000083.3:c.490T>C MANE Select	NP_000074.3:p.Trp164Arg
NR_046453.2:n.592T>C