Canonical Allele Identifier: CA168255835

Gene: CLCN1

Linked Data

• dbSNP Id: rs980845093
• gnomAD v4: 7-143321477-C-T
• MyVariant Identifiers: chr7:g.143018570C>T (hg19) ; chr7:g.143321477C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321477C>T , CM000669.2:g.143321477C>T	GRCh38
NC_000007.13:g.143018570C>T , CM000669.1:g.143018570C>T	GRCh37
NC_000007.12:g.142728692C>T	NCBI36
NG_009815.1:g.10352C>T
NG_009815.2:g.10352C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.546C>T	ENSP00000498052.2:p.Ile182=
ENST00000343257.7:c.546C>T MANE Select	ENSP00000339867.2:p.Ile182=
ENST00000432192.6:c.314C>T
ENST00000650516.1:c.546C>T	ENSP00000498052.1:p.Ile182=
ENST00000343257.6:c.546C>T	ENSP00000339867.2:p.Ile182=
ENST00000432192.5:c.4C>T
ENST00000455478.5:c.4C>T
ENST00000495612.1:n.4C>T
NM_000083.2:c.546C>T	NP_000074.2:p.Ile182=
NR_046453.1:n.633C>T
XM_011515781.1:c.546C>T	XP_011514083.1:p.Ile182=
XM_017011739.1:c.253C>T	XP_016867228.1:p.Leu85Phe
XM_017011740.1:c.253C>T	XP_016867229.1:p.Leu85Phe
NM_000083.3:c.546C>T MANE Select	NP_000074.3:p.Ile182=
NR_046453.2:n.648C>T