Canonical Allele Identifier: CA369641551

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143027897T>A (hg19) ; chr7:g.143330804T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143330804T>A , CM000669.2:g.143330804T>A	GRCh38
NC_000007.13:g.143027897T>A , CM000669.1:g.143027897T>A	GRCh37
NC_000007.12:g.142738019T>A	NCBI36
NG_009815.1:g.19679T>A
NG_009815.2:g.19679T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.886T>A	ENSP00000498052.2:p.Tyr296Asn
ENST00000343257.7:c.886T>A MANE Select	ENSP00000339867.2:p.Tyr296Asn
ENST00000432192.6:c.710T>A
ENST00000455478.6:c.474T>A	ENSP00000400027.2:n.474T>A
ENST00000650516.1:c.886T>A	ENSP00000498052.1:p.Tyr296Asn
ENST00000343257.6:c.886T>A	ENSP00000339867.2:p.Tyr296Asn
ENST00000432192.5:c.400T>A
ENST00000455478.5:c.478T>A
ENST00000495612.1:n.187T>A
NM_000083.2:c.886T>A	NP_000074.2:p.Tyr296Asn
NR_046453.1:n.976T>A
XM_011515781.1:c.886T>A	XP_011514083.1:p.Tyr296Asn
XM_017011739.1:c.436T>A	XP_016867228.1:p.Tyr146Asn
XM_017011740.1:c.436T>A	XP_016867229.1:p.Tyr146Asn
NM_000083.3:c.886T>A MANE Select	NP_000074.3:p.Tyr296Asn
NR_046453.2:n.991T>A