Canonical Allele Identifier: CA4537744

Gene: CLCN1

Linked Data

• dbSNP Id: rs751703867
• ExAC: 7:143048641 C / T
• gnomAD v2: 7-143048641-C-T
• gnomAD v3: 7-143351548-C-T
• gnomAD v4: 7-143351548-C-T
• MyVariant Identifiers: chr7:g.143048641C>T (hg19) ; chr7:g.143351548C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351548C>T , CM000669.2:g.143351548C>T	GRCh38
NC_000007.13:g.143048641C>T , CM000669.1:g.143048641C>T	GRCh37
NC_000007.12:g.142758763C>T	NCBI36
NG_009815.1:g.40423C>T
NG_009815.2:g.40423C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.2596-46C>T	ENSP00000498052.2:n.2596-46C>T
ENST00000343257.7:c.2596-46C>T MANE Select	ENSP00000339867.2:n.2596-46C>T
ENST00000432192.6:c.2420-46C>T
ENST00000343257.6:c.2596-46C>T	ENSP00000339867.2:n.2596-46C>T
NM_000083.2:c.2596-46C>T	NP_000074.2:n.2596-46C>T
NR_046453.1:n.2536-46C>T
XM_011515781.1:c.2620-46C>T	XP_011514083.1:n.2620-46C>T
XM_011515782.1:c.1342-46C>T	XP_011514084.1:n.1342-46C>T
XM_011515782.2:c.1342-46C>T	XP_011514084.1:n.1342-46C>T
XM_017011739.1:c.2170-46C>T	XP_016867228.1:n.2170-46C>T
XM_017011740.1:c.2146-46C>T	XP_016867229.1:n.2146-46C>T
NM_000083.3:c.2596-46C>T MANE Select	NP_000074.3:n.2596-46C>T
NR_046453.2:n.2551-46C>T