Canonical Allele Identifier: CA4537801

Gene: CLCN1

Linked Data

• dbSNP Id: rs753877377
• ExAC: 7:143048942 T / C
• gnomAD v4: 7-143351849-T-C
• MyVariant Identifiers: chr7:g.143048942T>C (hg19) ; chr7:g.143351849T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351849T>C , CM000669.2:g.143351849T>C	GRCh38
NC_000007.13:g.143048942T>C , CM000669.1:g.143048942T>C	GRCh37
NC_000007.12:g.142759064T>C	NCBI36
NG_009815.1:g.40724T>C
NG_009815.2:g.40724T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2851T>C	ENSP00000498052.2:p.Leu951=
ENST00000343257.7:c.2851T>C MANE Select	ENSP00000339867.2:p.Leu951=
ENST00000343257.6:c.2851T>C	ENSP00000339867.2:p.Leu951=
NM_000083.2:c.2851T>C	NP_000074.2:p.Leu951=
NR_046453.1:n.2791T>C
XM_011515781.1:c.2875T>C	XP_011514083.1:p.Leu959=
XM_011515782.1:c.1597T>C	XP_011514084.1:p.Leu533=
XM_011515782.2:c.1597T>C	XP_011514084.1:p.Leu533=
XM_017011739.1:c.2425T>C	XP_016867228.1:p.Leu809=
XM_017011740.1:c.2401T>C	XP_016867229.1:p.Leu801=
NM_000083.3:c.2851T>C MANE Select	NP_000074.3:p.Leu951=
NR_046453.2:n.2806T>C