Canonical Allele Identifier: CA369653756

Gene: CLCN1

Linked Data

• dbSNP Id: rs867539633
• gnomAD v4: 7-143351759-G-T
• MyVariant Identifiers: chr7:g.143048852G>T (hg19) ; chr7:g.143351759G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351759G>T , CM000669.2:g.143351759G>T	GRCh38
NC_000007.13:g.143048852G>T , CM000669.1:g.143048852G>T	GRCh37
NC_000007.12:g.142758974G>T	NCBI36
NG_009815.1:g.40634G>T
NG_009815.2:g.40634G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2761G>T	ENSP00000498052.2:p.Asp921Tyr
ENST00000343257.7:c.2761G>T MANE Select	ENSP00000339867.2:p.Asp921Tyr
ENST00000343257.6:c.2761G>T	ENSP00000339867.2:p.Asp921Tyr
NM_000083.2:c.2761G>T	NP_000074.2:p.Asp921Tyr
NR_046453.1:n.2701G>T
XM_011515781.1:c.2785G>T	XP_011514083.1:p.Asp929Tyr
XM_011515782.1:c.1507G>T	XP_011514084.1:p.Asp503Tyr
XM_011515782.2:c.1507G>T	XP_011514084.1:p.Asp503Tyr
XM_017011739.1:c.2335G>T	XP_016867228.1:p.Asp779Tyr
XM_017011740.1:c.2311G>T	XP_016867229.1:p.Asp771Tyr
NM_000083.3:c.2761G>T MANE Select	NP_000074.3:p.Asp921Tyr
NR_046453.2:n.2716G>T