Canonical Allele Identifier: CA369643846

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143029845T>A (hg19) ; chr7:g.143332752T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143332752T>A , CM000669.2:g.143332752T>A	GRCh38
NC_000007.13:g.143029845T>A , CM000669.1:g.143029845T>A	GRCh37
NC_000007.12:g.142739967T>A	NCBI36
NG_009815.1:g.21627T>A
NG_009815.2:g.21627T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1280T>A	ENSP00000498052.2:p.Leu427Ter
ENST00000343257.7:c.1280T>A MANE Select	ENSP00000339867.2:p.Leu427Ter
ENST00000432192.6:c.1104T>A
ENST00000343257.6:c.1280T>A	ENSP00000339867.2:p.Leu427Ter
NM_000083.2:c.1280T>A	NP_000074.2:p.Leu427Ter
NR_046453.1:n.1341+249T>A
XM_011515781.1:c.1304T>A	XP_011514083.1:p.Leu435Ter
XM_011515782.1:c.26T>A	XP_011514084.1:p.Leu9Ter
XM_011515782.2:c.26T>A	XP_011514084.1:p.Leu9Ter
XM_017011739.1:c.854T>A	XP_016867228.1:p.Leu285Ter
XM_017011740.1:c.830T>A	XP_016867229.1:p.Leu277Ter
NM_000083.3:c.1280T>A MANE Select	NP_000074.3:p.Leu427Ter
NR_046453.2:n.1356+249T>A