Canonical Allele Identifier: CA4536924
Community Standard Title: NM_000083.3(CLCN1):c.395G>T (p.Ser132Ile)
Gene: CLCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.143320757G>T , CM000669.2:g.143320757G>T GRCh38
NC_000007.13:g.143017850G>T , CM000669.1:g.143017850G>T GRCh37
NC_000007.12:g.142727972G>T NCBI36
NG_009815.1:g.9632G>T
NG_009815.2:g.9632G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000083.3:c.395G>T MANE Select NP_000074.3:p.Ser132Ile
ENST00000343257.7:c.395G>T MANE Select ENSP00000339867.2:p.Ser132Ile
NM_000083.2:c.395G>T NP_000074.2:p.Ser132Ile
NR_046453.1:n.482G>T
NR_046453.2:n.497G>T
ENST00000343257.6:c.395G>T ENSP00000339867.2:p.Ser132Ile
ENST00000432192.6:c.163G>T
ENST00000650516.1:c.395G>T ENSP00000498052.1:p.Ser132Ile
ENST00000650516.2:c.395G>T ENSP00000498052.2:p.Ser132Ile
XM_011515781.1:c.395G>T XP_011514083.1:p.Ser132Ile
XM_017011739.1:c.102G>T XP_016867228.1:p.Gln34His
XM_017011740.1:c.102G>T XP_016867229.1:p.Gln34His