Canonical Allele Identifier: CA369653598

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143048774A>T (hg19) ; chr7:g.143351681A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143351681A>T , CM000669.2:g.143351681A>T	GRCh38
NC_000007.13:g.143048774A>T , CM000669.1:g.143048774A>T	GRCh37
NC_000007.12:g.142758896A>T	NCBI36
NG_009815.1:g.40556A>T
NG_009815.2:g.40556A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.2683A>T	ENSP00000498052.2:p.Lys895Ter
ENST00000343257.7:c.2683A>T MANE Select	ENSP00000339867.2:p.Lys895Ter
ENST00000432192.6:c.2507A>T
ENST00000343257.6:c.2683A>T	ENSP00000339867.2:p.Lys895Ter
NM_000083.2:c.2683A>T	NP_000074.2:p.Lys895Ter
NR_046453.1:n.2623A>T
XM_011515781.1:c.2707A>T	XP_011514083.1:p.Lys903Ter
XM_011515782.1:c.1429A>T	XP_011514084.1:p.Lys477Ter
XM_011515782.2:c.1429A>T	XP_011514084.1:p.Lys477Ter
XM_017011739.1:c.2257A>T	XP_016867228.1:p.Lys753Ter
XM_017011740.1:c.2233A>T	XP_016867229.1:p.Lys745Ter
NM_000083.3:c.2683A>T MANE Select	NP_000074.3:p.Lys895Ter
NR_046453.2:n.2638A>T