Canonical Allele Identifier: CA834513386

Gene: CLCN1

Linked Data

• dbSNP Id: rs1198417598
• gnomAD v3: 7-143332673-A-G
• gnomAD v4: 7-143332673-A-G
• MyVariant Identifiers: chr7:g.143029766A>G (hg19) ; chr7:g.143332673A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143332673A>G , CM000669.2:g.143332673A>G	GRCh38
NC_000007.13:g.143029766A>G , CM000669.1:g.143029766A>G	GRCh37
NC_000007.12:g.142739888A>G	NCBI36
NG_009815.1:g.21548A>G
NG_009815.2:g.21548A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1252-51A>G	ENSP00000498052.2:n.1252-51A>G
ENST00000343257.7:c.1252-51A>G MANE Select	ENSP00000339867.2:n.1252-51A>G
ENST00000432192.6:c.1076-51A>G
ENST00000343257.6:c.1252-51A>G	ENSP00000339867.2:n.1252-51A>G
NM_000083.2:c.1252-51A>G	NP_000074.2:n.1252-51A>G
NR_046453.1:n.1341+170A>G
XM_011515781.1:c.1276-51A>G	XP_011514083.1:n.1276-51A>G
XM_011515782.1:c.-3-51A>G	XP_011514084.1:n.-3-51A>G
XM_011515782.2:c.-3-51A>G	XP_011514084.1:n.-3-51A>G
XM_017011739.1:c.826-51A>G	XP_016867228.1:n.826-51A>G
XM_017011740.1:c.802-51A>G	XP_016867229.1:n.802-51A>G
NM_000083.3:c.1252-51A>G MANE Select	NP_000074.3:n.1252-51A>G
NR_046453.2:n.1356+170A>G