Canonical Allele Identifier: CA369645308

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143036371C>T (hg19) ; chr7:g.143339278C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143339278C>T , CM000669.2:g.143339278C>T	GRCh38
NC_000007.13:g.143036371C>T , CM000669.1:g.143036371C>T	GRCh37
NC_000007.12:g.142746493C>T	NCBI36
NG_009815.1:g.28153C>T
NG_009815.2:g.28153C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1427C>T	ENSP00000498052.2:p.Thr476Ile
ENST00000343257.7:c.1427C>T MANE Select	ENSP00000339867.2:p.Thr476Ile
ENST00000432192.6:c.1251C>T
ENST00000343257.6:c.1427C>T	ENSP00000339867.2:p.Thr476Ile
NM_000083.2:c.1427C>T	NP_000074.2:p.Thr476Ile
NR_046453.1:n.1367C>T
XM_011515781.1:c.1451C>T	XP_011514083.1:p.Thr484Ile
XM_011515782.1:c.173C>T	XP_011514084.1:p.Thr58Ile
XM_011515782.2:c.173C>T	XP_011514084.1:p.Thr58Ile
XM_017011739.1:c.1001C>T	XP_016867228.1:p.Thr334Ile
XM_017011740.1:c.977C>T	XP_016867229.1:p.Thr326Ile
NM_000083.3:c.1427C>T MANE Select	NP_000074.3:p.Thr476Ile
NR_046453.2:n.1382C>T