Canonical Allele Identifier: CA369684803

Gene: CLCN1

Linked Data

• MyVariant Identifiers: chr7:g.143018889A>T (hg19) ; chr7:g.143321796A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143321796A>T , CM000669.2:g.143321796A>T	GRCh38
NC_000007.13:g.143018889A>T , CM000669.1:g.143018889A>T	GRCh37
NC_000007.12:g.142729011A>T	NCBI36
NG_009815.1:g.10671A>T
NG_009815.2:g.10671A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650516.2:c.644A>T	ENSP00000498052.2:p.Lys215Met
ENST00000343257.7:c.644A>T MANE Select	ENSP00000339867.2:p.Lys215Met
ENST00000432192.6:c.412A>T
ENST00000455478.6:c.98A>T	ENSP00000400027.2:p.Lys33Met
ENST00000650516.1:c.644A>T	ENSP00000498052.1:p.Lys215Met
ENST00000343257.6:c.644A>T	ENSP00000339867.2:p.Lys215Met
ENST00000432192.5:c.102A>T
ENST00000455478.5:c.102A>T
ENST00000495612.1:n.102A>T
NM_000083.2:c.644A>T	NP_000074.2:p.Lys215Met
NR_046453.1:n.731A>T
XM_011515781.1:c.644A>T	XP_011514083.1:p.Lys215Met
XM_017011739.1:c.351A>T	XP_016867228.1:p.Gln117His
XM_017011740.1:c.351A>T	XP_016867229.1:p.Gln117His
NM_000083.3:c.644A>T MANE Select	NP_000074.3:p.Lys215Met
NR_046453.2:n.746A>T