Canonical Allele Identifier: CA2685378926

Gene: CLCN1

Linked Data

• gnomAD v4: 7-143339458-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143339458G>T , CM000669.2:g.143339458G>T	GRCh38
NC_000007.13:g.143036551G>T , CM000669.1:g.143036551G>T	GRCh37
NC_000007.12:g.142746673G>T	NCBI36
NG_009815.1:g.28333G>T
NG_009815.2:g.28333G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.1472-53G>T	ENSP00000498052.2:n.1472-53G>T
ENST00000343257.7:c.1472-53G>T MANE Select	ENSP00000339867.2:n.1472-53G>T
ENST00000432192.6:c.1296-53G>T
ENST00000343257.6:c.1472-53G>T	ENSP00000339867.2:n.1472-53G>T
NM_000083.2:c.1472-53G>T	NP_000074.2:n.1472-53G>T
NR_046453.1:n.1412-53G>T
XM_011515781.1:c.1496-53G>T	XP_011514083.1:n.1496-53G>T
XM_011515782.1:c.218-53G>T	XP_011514084.1:n.218-53G>T
XM_011515782.2:c.218-53G>T	XP_011514084.1:n.218-53G>T
XM_017011739.1:c.1046-53G>T	XP_016867228.1:n.1046-53G>T
XM_017011740.1:c.1022-53G>T	XP_016867229.1:n.1022-53G>T
NM_000083.3:c.1472-53G>T MANE Select	NP_000074.3:n.1472-53G>T
NR_046453.2:n.1427-53G>T