Canonical Allele Identifier: CA369643841

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143029844T>G (hg19) ; chr7:g.143332751T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143332751T>G , CM000669.2:g.143332751T>G	GRCh38
NC_000007.13:g.143029844T>G , CM000669.1:g.143029844T>G	GRCh37
NC_000007.12:g.142739966T>G	NCBI36
NG_009815.1:g.21626T>G
NG_009815.2:g.21626T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1279T>G	ENSP00000498052.2:p.Leu427Val
ENST00000343257.7:c.1279T>G MANE Select	ENSP00000339867.2:p.Leu427Val
ENST00000432192.6:c.1103T>G
ENST00000343257.6:c.1279T>G	ENSP00000339867.2:p.Leu427Val
NM_000083.2:c.1279T>G	NP_000074.2:p.Leu427Val
NR_046453.1:n.1341+248T>G
XM_011515781.1:c.1303T>G	XP_011514083.1:p.Leu435Val
XM_011515782.1:c.25T>G	XP_011514084.1:p.Leu9Val
XM_011515782.2:c.25T>G	XP_011514084.1:p.Leu9Val
XM_017011739.1:c.853T>G	XP_016867228.1:p.Leu285Val
XM_017011740.1:c.829T>G	XP_016867229.1:p.Leu277Val
NM_000083.3:c.1279T>G MANE Select	NP_000074.3:p.Leu427Val
NR_046453.2:n.1356+248T>G