Canonical Allele Identifier: CA356273418
Gene: CYTL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.5015163A>C , CM000666.2:g.5015163A>C GRCh38
NC_000004.11:g.5016890A>C , CM000666.1:g.5016890A>C GRCh37
NC_000004.10:g.5067791A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000307746.9:c.399T>G MANE Select ENSP00000303550.4:p.Asp133Glu
ENST00000307746.8:c.399T>G ENSP00000303550.4:p.Asp133Glu
ENST00000506508.1:c.217T>G
ENST00000509419.1:c.266T>G
NM_018659.2:c.399T>G NP_061129.1:p.Asp133Glu
XR_925085.1:n.149-4760A>C
XR_925086.1:n.149-4760A>C
XR_925087.1:n.149-4760A>C
XM_017008299.1:c.*49T>G XP_016863788.1:n.*49T>G
NM_018659.3:c.399T>G MANE Select NP_061129.1:p.Asp133Glu