Canonical Allele Identifier: CA369646344

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143039022G>C (hg19) ; chr7:g.143341929G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143341929G>C , CM000669.2:g.143341929G>C	GRCh38
NC_000007.13:g.143039022G>C , CM000669.1:g.143039022G>C	GRCh37
NC_000007.12:g.142749144G>C	NCBI36
NG_009815.1:g.30804G>C
NG_009815.2:g.30804G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1583G>C	ENSP00000498052.2:p.Gly528Ala
ENST00000343257.7:c.1583G>C MANE Select	ENSP00000339867.2:p.Gly528Ala
ENST00000432192.6:c.1407G>C
ENST00000343257.6:c.1583G>C	ENSP00000339867.2:p.Gly528Ala
NM_000083.2:c.1583G>C	NP_000074.2:p.Gly528Ala
NR_046453.1:n.1523G>C
XM_011515781.1:c.1607G>C	XP_011514083.1:p.Gly536Ala
XM_011515782.1:c.329G>C	XP_011514084.1:p.Gly110Ala
XM_011515782.2:c.329G>C	XP_011514084.1:p.Gly110Ala
XM_017011739.1:c.1157G>C	XP_016867228.1:p.Gly386Ala
XM_017011740.1:c.1133G>C	XP_016867229.1:p.Gly378Ala
NM_000083.3:c.1583G>C MANE Select	NP_000074.3:p.Gly528Ala
NR_046453.2:n.1538G>C