Canonical Allele Identifier: CA369684839

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143018895T>C (hg19) ; chr7:g.143321802T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321802T>C , CM000669.2:g.143321802T>C	GRCh38
NC_000007.13:g.143018895T>C , CM000669.1:g.143018895T>C	GRCh37
NC_000007.12:g.142729017T>C	NCBI36
NG_009815.1:g.10677T>C
NG_009815.2:g.10677T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.650T>C	ENSP00000498052.2:p.Val217Ala
ENST00000343257.7:c.650T>C MANE Select	ENSP00000339867.2:p.Val217Ala
ENST00000432192.6:c.418T>C
ENST00000455478.6:c.104T>C	ENSP00000400027.2:p.Val35Ala
ENST00000650516.1:c.650T>C	ENSP00000498052.1:p.Val217Ala
ENST00000343257.6:c.650T>C	ENSP00000339867.2:p.Val217Ala
ENST00000432192.5:c.108T>C
ENST00000455478.5:c.108T>C
ENST00000495612.1:n.108T>C
NM_000083.2:c.650T>C	NP_000074.2:p.Val217Ala
NR_046453.1:n.737T>C
XM_011515781.1:c.650T>C	XP_011514083.1:p.Val217Ala
XM_017011739.1:c.357T>C	XP_016867228.1:p.Cys119=
XM_017011740.1:c.357T>C	XP_016867229.1:p.Cys119=
NM_000083.3:c.650T>C MANE Select	NP_000074.3:p.Val217Ala
NR_046453.2:n.752T>C