Canonical Allele Identifier: CA369652683

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143047565A>T (hg19) ; chr7:g.143350472A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143350472A>T , CM000669.2:g.143350472A>T	GRCh38
NC_000007.13:g.143047565A>T , CM000669.1:g.143047565A>T	GRCh37
NC_000007.12:g.142757687A>T	NCBI36
NG_009815.1:g.39347A>T
NG_009815.2:g.39347A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.2504A>T	ENSP00000498052.2:p.His835Leu
ENST00000343257.7:c.2504A>T MANE Select	ENSP00000339867.2:p.His835Leu
ENST00000432192.6:c.2328A>T
ENST00000343257.6:c.2504A>T	ENSP00000339867.2:p.His835Leu
NM_000083.2:c.2504A>T	NP_000074.2:p.His835Leu
NR_046453.1:n.2444A>T
XM_011515781.1:c.2528A>T	XP_011514083.1:p.His843Leu
XM_011515782.1:c.1250A>T	XP_011514084.1:p.His417Leu
XM_011515782.2:c.1250A>T	XP_011514084.1:p.His417Leu
XM_017011739.1:c.2078A>T	XP_016867228.1:p.His693Leu
XM_017011740.1:c.2054A>T	XP_016867229.1:p.His685Leu
NM_000083.3:c.2504A>T MANE Select	NP_000074.3:p.His835Leu
NR_046453.2:n.2459A>T