Canonical Allele Identifier: CA1748881653

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321726C= , CM000669.2:g.143321726C=	GRCh38
NC_000007.13:g.143018819C= , CM000669.1:g.143018819C=	GRCh37
NC_000007.12:g.142728941C=	NCBI36
NG_009815.1:g.10601C=
NG_009815.2:g.10601C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.574C=	ENSP00000498052.2:p.Pro192=
ENST00000343257.7:c.574C= MANE Select	ENSP00000339867.2:p.Pro192=
ENST00000432192.6:c.342C=
ENST00000455478.6:c.28C=	ENSP00000400027.2:p.Pro10=
ENST00000650516.1:c.574C=	ENSP00000498052.1:p.Pro192=
ENST00000343257.6:c.574C=	ENSP00000339867.2:p.Pro192=
ENST00000432192.5:c.32C=
ENST00000455478.5:c.32C=
ENST00000495612.1:n.32C=
NM_000083.2:c.574C=	NP_000074.2:p.Pro192=
NR_046453.1:n.661C=
XM_011515781.1:c.574C=	XP_011514083.1:p.Pro192=
XM_017011739.1:c.281C=	XP_016867228.1:p.Pro94=
XM_017011740.1:c.281C=	XP_016867229.1:p.Pro94=
NM_000083.3:c.574C= MANE Select	NP_000074.3:p.Pro192=
NR_046453.2:n.676C=