Canonical Allele Identifier: CA369646446

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143039074T>G (hg19) ; chr7:g.143341981T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143341981T>G , CM000669.2:g.143341981T>G	GRCh38
NC_000007.13:g.143039074T>G , CM000669.1:g.143039074T>G	GRCh37
NC_000007.12:g.142749196T>G	NCBI36
NG_009815.1:g.30856T>G
NG_009815.2:g.30856T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1635T>G	ENSP00000498052.2:p.Ile545Met
ENST00000343257.7:c.1635T>G MANE Select	ENSP00000339867.2:p.Ile545Met
ENST00000432192.6:c.1459T>G
ENST00000343257.6:c.1635T>G	ENSP00000339867.2:p.Ile545Met
NM_000083.2:c.1635T>G	NP_000074.2:p.Ile545Met
NR_046453.1:n.1575T>G
XM_011515781.1:c.1659T>G	XP_011514083.1:p.Ile553Met
XM_011515782.1:c.381T>G	XP_011514084.1:p.Ile127Met
XM_011515782.2:c.381T>G	XP_011514084.1:p.Ile127Met
XM_017011739.1:c.1209T>G	XP_016867228.1:p.Ile403Met
XM_017011740.1:c.1185T>G	XP_016867229.1:p.Ile395Met
NM_000083.3:c.1635T>G MANE Select	NP_000074.3:p.Ile545Met
NR_046453.2:n.1590T>G