Canonical Allele Identifier: CA369653167

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143047682C>T (hg19) ; chr7:g.143350589C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143350589C>T , CM000669.2:g.143350589C>T	GRCh38
NC_000007.13:g.143047682C>T , CM000669.1:g.143047682C>T	GRCh37
NC_000007.12:g.142757804C>T	NCBI36
NG_009815.1:g.39464C>T
NG_009815.2:g.39464C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.2530C>T	ENSP00000498052.2:p.Leu844Phe
ENST00000343257.7:c.2530C>T MANE Select	ENSP00000339867.2:p.Leu844Phe
ENST00000432192.6:c.2354C>T
ENST00000343257.6:c.2530C>T	ENSP00000339867.2:p.Leu844Phe
NM_000083.2:c.2530C>T	NP_000074.2:p.Leu844Phe
NR_046453.1:n.2470C>T
XM_011515781.1:c.2554C>T	XP_011514083.1:p.Leu852Phe
XM_011515782.1:c.1276C>T	XP_011514084.1:p.Leu426Phe
XM_011515782.2:c.1276C>T	XP_011514084.1:p.Leu426Phe
XM_017011739.1:c.2104C>T	XP_016867228.1:p.Leu702Phe
XM_017011740.1:c.2080C>T	XP_016867229.1:p.Leu694Phe
NM_000083.3:c.2530C>T MANE Select	NP_000074.3:p.Leu844Phe
NR_046453.2:n.2485C>T