Canonical Allele Identifier: CA369653674

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143048810T>C (hg19) ; chr7:g.143351717T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351717T>C , CM000669.2:g.143351717T>C	GRCh38
NC_000007.13:g.143048810T>C , CM000669.1:g.143048810T>C	GRCh37
NC_000007.12:g.142758932T>C	NCBI36
NG_009815.1:g.40592T>C
NG_009815.2:g.40592T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2719T>C	ENSP00000498052.2:p.Trp907Arg
ENST00000343257.7:c.2719T>C MANE Select	ENSP00000339867.2:p.Trp907Arg
ENST00000432192.6:c.2543T>C
ENST00000343257.6:c.2719T>C	ENSP00000339867.2:p.Trp907Arg
NM_000083.2:c.2719T>C	NP_000074.2:p.Trp907Arg
NR_046453.1:n.2659T>C
XM_011515781.1:c.2743T>C	XP_011514083.1:p.Trp915Arg
XM_011515782.1:c.1465T>C	XP_011514084.1:p.Trp489Arg
XM_011515782.2:c.1465T>C	XP_011514084.1:p.Trp489Arg
XM_017011739.1:c.2293T>C	XP_016867228.1:p.Trp765Arg
XM_017011740.1:c.2269T>C	XP_016867229.1:p.Trp757Arg
NM_000083.3:c.2719T>C MANE Select	NP_000074.3:p.Trp907Arg
NR_046453.2:n.2674T>C