Canonical Allele Identifier: CA369646634

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143039161G>C (hg19) ; chr7:g.143342068G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143342068G>C , CM000669.2:g.143342068G>C	GRCh38
NC_000007.13:g.143039161G>C , CM000669.1:g.143039161G>C	GRCh37
NC_000007.12:g.142749283G>C	NCBI36
NG_009815.1:g.30943G>C
NG_009815.2:g.30943G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.1722G>C	ENSP00000498052.2:p.Gln574His
ENST00000343257.7:c.1722G>C MANE Select	ENSP00000339867.2:p.Gln574His
ENST00000432192.6:c.1546G>C
ENST00000343257.6:c.1722G>C	ENSP00000339867.2:p.Gln574His
NM_000083.2:c.1722G>C	NP_000074.2:p.Gln574His
NR_046453.1:n.1662G>C
XM_011515781.1:c.1746G>C	XP_011514083.1:p.Gln582His
XM_011515782.1:c.468G>C	XP_011514084.1:p.Gln156His
XM_011515782.2:c.468G>C	XP_011514084.1:p.Gln156His
XM_017011739.1:c.1296G>C	XP_016867228.1:p.Gln432His
XM_017011740.1:c.1272G>C	XP_016867229.1:p.Gln424His
NM_000083.3:c.1722G>C MANE Select	NP_000074.3:p.Gln574His
NR_046453.2:n.1677G>C