Canonical Allele Identifier: CA369654332

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143049043T>A (hg19) ; chr7:g.143351950T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351950T>A , CM000669.2:g.143351950T>A	GRCh38
NC_000007.13:g.143049043T>A , CM000669.1:g.143049043T>A	GRCh37
NC_000007.12:g.142759165T>A	NCBI36
NG_009815.1:g.40825T>A
NG_009815.2:g.40825T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2952T>A	ENSP00000498052.2:p.Asp984Glu
ENST00000343257.7:c.2952T>A MANE Select	ENSP00000339867.2:p.Asp984Glu
ENST00000343257.6:c.2952T>A	ENSP00000339867.2:p.Asp984Glu
NM_000083.2:c.2952T>A	NP_000074.2:p.Asp984Glu
NR_046453.1:n.2892T>A
XM_011515781.1:c.2976T>A	XP_011514083.1:p.Asp992Glu
XM_011515782.1:c.1698T>A	XP_011514084.1:p.Asp566Glu
XM_011515782.2:c.1698T>A	XP_011514084.1:p.Asp566Glu
XM_017011739.1:c.2526T>A	XP_016867228.1:p.Asp842Glu
XM_017011740.1:c.2502T>A	XP_016867229.1:p.Asp834Glu
NM_000083.3:c.2952T>A MANE Select	NP_000074.3:p.Asp984Glu
NR_046453.2:n.2907T>A