Canonical Allele Identifier: CA369653176

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143047686G>A (hg19) ; chr7:g.143350593G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143350593G>A , CM000669.2:g.143350593G>A	GRCh38
NC_000007.13:g.143047686G>A , CM000669.1:g.143047686G>A	GRCh37
NC_000007.12:g.142757808G>A	NCBI36
NG_009815.1:g.39468G>A
NG_009815.2:g.39468G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2534G>A	ENSP00000498052.2:p.Gly845Asp
ENST00000343257.7:c.2534G>A MANE Select	ENSP00000339867.2:p.Gly845Asp
ENST00000432192.6:c.2358G>A
ENST00000343257.6:c.2534G>A	ENSP00000339867.2:p.Gly845Asp
NM_000083.2:c.2534G>A	NP_000074.2:p.Gly845Asp
NR_046453.1:n.2474G>A
XM_011515781.1:c.2558G>A	XP_011514083.1:p.Gly853Asp
XM_011515782.1:c.1280G>A	XP_011514084.1:p.Gly427Asp
XM_011515782.2:c.1280G>A	XP_011514084.1:p.Gly427Asp
XM_017011739.1:c.2108G>A	XP_016867228.1:p.Gly703Asp
XM_017011740.1:c.2084G>A	XP_016867229.1:p.Gly695Asp
NM_000083.3:c.2534G>A MANE Select	NP_000074.3:p.Gly845Asp
NR_046453.2:n.2489G>A