Canonical Allele Identifier: CA458542348

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143048758C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351665C>T , CM000669.2:g.143351665C>T	GRCh38
NC_000007.13:g.143048758C>T , CM000669.1:g.143048758C>T	GRCh37
NC_000007.12:g.142758880C>T	NCBI36
NG_009815.1:g.40540C>T
NG_009815.2:g.40540C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2667C>T	ENSP00000498052.2:p.Asn889=
ENST00000343257.7:c.2667C>T MANE Select	ENSP00000339867.2:p.Asn889=
ENST00000432192.6:c.2491C>T
ENST00000343257.6:c.2667C>T	ENSP00000339867.2:p.Asn889=
NM_000083.2:c.2667C>T	NP_000074.2:p.Asn889=
NR_046453.1:n.2607C>T
XM_011515781.1:c.2691C>T	XP_011514083.1:p.Asn897=
XM_011515782.1:c.1413C>T	XP_011514084.1:p.Asn471=
XM_011515782.2:c.1413C>T	XP_011514084.1:p.Asn471=
XM_017011739.1:c.2241C>T	XP_016867228.1:p.Asn747=
XM_017011740.1:c.2217C>T	XP_016867229.1:p.Asn739=
NM_000083.3:c.2667C>T MANE Select	NP_000074.3:p.Asn889=
NR_046453.2:n.2622C>T