Canonical Allele Identifier: CA388305776
Gene: CLN5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.76992000G>T , CM000675.2:g.76992000G>T GRCh38
NC_000013.10:g.77566135G>T , CM000675.1:g.77566135G>T GRCh37
NC_000013.9:g.76464136G>T NCBI36
NG_009064.1:g.5077G>T , LRG_692:g.5077G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000636183.2:c.-99G>T ENSP00000490181.2:n.-99G>T
ENST00000377453.7:c.49G>T ENSP00000366673.3:p.Gly17Trp
NM_006493.2:c.49G>T , LRG_692t1:c.49G>T NP_006484.1:p.Gly17Trp
XM_011534917.1:c.49G>T XP_011533219.1:p.Gly17Trp