Canonical Allele Identifier: CA369687615

Gene: CLCN1

Linked Data

• gnomAD v4: 7-143324487-T-C
• MyVariant Identifiers: chr7:g.143021580T>C (hg19) ; chr7:g.143324487T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143324487T>C , CM000669.2:g.143324487T>C	GRCh38
NC_000007.13:g.143021580T>C , CM000669.1:g.143021580T>C	GRCh37
NC_000007.12:g.142731702T>C	NCBI36
NG_009815.1:g.13362T>C
NG_009815.2:g.13362T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.853+590T>C	ENSP00000498052.2:n.853+590T>C
ENST00000343257.7:c.848T>C MANE Select	ENSP00000339867.2:p.Leu283Pro
ENST00000432192.6:c.672T>C
ENST00000455478.6:c.436T>C	ENSP00000400027.2:n.436T>C
ENST00000650516.1:c.853+590T>C	ENSP00000498052.1:n.853+590T>C
ENST00000343257.6:c.848T>C	ENSP00000339867.2:p.Leu283Pro
ENST00000432192.5:c.362T>C
ENST00000455478.5:c.440T>C
ENST00000495612.1:n.154+2639T>C
NM_000083.2:c.848T>C	NP_000074.2:p.Leu283Pro
NR_046453.1:n.938T>C
XM_011515781.1:c.853+590T>C	XP_011514083.1:n.853+590T>C
XM_017011739.1:c.403+2639T>C	XP_016867228.1:n.403+2639T>C
XM_017011740.1:c.403+2639T>C	XP_016867229.1:n.403+2639T>C
NM_000083.3:c.848T>C MANE Select	NP_000074.3:p.Leu283Pro
NR_046453.2:n.953T>C