Canonical Allele Identifier: CA369644436

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143029968T>A (hg19) ; chr7:g.143332875T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143332875T>A , CM000669.2:g.143332875T>A	GRCh38
NC_000007.13:g.143029968T>A , CM000669.1:g.143029968T>A	GRCh37
NC_000007.12:g.142740090T>A	NCBI36
NG_009815.1:g.21750T>A
NG_009815.2:g.21750T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.1401+2T>A	ENSP00000498052.2:n.1401+2T>A
ENST00000343257.7:c.1401+2T>A MANE Select	ENSP00000339867.2:n.1401+2T>A
ENST00000432192.6:c.1225+2T>A
ENST00000343257.6:c.1401+2T>A	ENSP00000339867.2:n.1401+2T>A
NM_000083.2:c.1401+2T>A	NP_000074.2:n.1401+2T>A
NR_046453.1:n.1341+372T>A
XM_011515781.1:c.1425+2T>A	XP_011514083.1:n.1425+2T>A
XM_011515782.1:c.147+2T>A	XP_011514084.1:n.147+2T>A
XM_011515782.2:c.147+2T>A	XP_011514084.1:n.147+2T>A
XM_017011739.1:c.975+2T>A	XP_016867228.1:n.975+2T>A
XM_017011740.1:c.951+2T>A	XP_016867229.1:n.951+2T>A
NM_000083.3:c.1401+2T>A MANE Select	NP_000074.3:n.1401+2T>A
NR_046453.2:n.1356+372T>A