Canonical Allele Identifier: CA369653670

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143048808A>T (hg19) ; chr7:g.143351715A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351715A>T , CM000669.2:g.143351715A>T	GRCh38
NC_000007.13:g.143048808A>T , CM000669.1:g.143048808A>T	GRCh37
NC_000007.12:g.142758930A>T	NCBI36
NG_009815.1:g.40590A>T
NG_009815.2:g.40590A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2717A>T	ENSP00000498052.2:p.Asn906Ile
ENST00000343257.7:c.2717A>T MANE Select	ENSP00000339867.2:p.Asn906Ile
ENST00000432192.6:c.2541A>T
ENST00000343257.6:c.2717A>T	ENSP00000339867.2:p.Asn906Ile
NM_000083.2:c.2717A>T	NP_000074.2:p.Asn906Ile
NR_046453.1:n.2657A>T
XM_011515781.1:c.2741A>T	XP_011514083.1:p.Asn914Ile
XM_011515782.1:c.1463A>T	XP_011514084.1:p.Asn488Ile
XM_011515782.2:c.1463A>T	XP_011514084.1:p.Asn488Ile
XM_017011739.1:c.2291A>T	XP_016867228.1:p.Asn764Ile
XM_017011740.1:c.2267A>T	XP_016867229.1:p.Asn756Ile
NM_000083.3:c.2717A>T MANE Select	NP_000074.3:p.Asn906Ile
NR_046453.2:n.2672A>T