Canonical Allele Identifier: CA1748889822

Gene: CLCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143332876A= , CM000669.2:g.143332876A=	GRCh38
NC_000007.13:g.143029969A= , CM000669.1:g.143029969A=	GRCh37
NC_000007.12:g.142740091A=	NCBI36
NG_009815.1:g.21751A=
NG_009815.2:g.21751A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000650516.2:c.1401+3A=	ENSP00000498052.2:n.1401+3A=
ENST00000343257.7:c.1401+3A= MANE Select	ENSP00000339867.2:n.1401+3A=
ENST00000432192.6:c.1225+3A=
ENST00000343257.6:c.1401+3A=	ENSP00000339867.2:n.1401+3A=
NM_000083.2:c.1401+3A=	NP_000074.2:n.1401+3A=
NR_046453.1:n.1341+373A=
XM_011515781.1:c.1425+3A=	XP_011514083.1:n.1425+3A=
XM_011515782.1:c.147+3A=	XP_011514084.1:n.147+3A=
XM_011515782.2:c.147+3A=	XP_011514084.1:n.147+3A=
XM_017011739.1:c.975+3A=	XP_016867228.1:n.975+3A=
XM_017011740.1:c.951+3A=	XP_016867229.1:n.951+3A=
NM_000083.3:c.1401+3A= MANE Select	NP_000074.3:n.1401+3A=
NR_046453.2:n.1356+373A=