Canonical Allele Identifier: CA356273423
Gene: CYTL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.5015165C>G , CM000666.2:g.5015165C>G GRCh38
NC_000004.11:g.5016892C>G , CM000666.1:g.5016892C>G GRCh37
NC_000004.10:g.5067793C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000307746.9:c.397G>C MANE Select ENSP00000303550.4:p.Asp133His
ENST00000307746.8:c.397G>C ENSP00000303550.4:p.Asp133His
ENST00000506508.1:c.215G>C
ENST00000509419.1:c.264G>C
NM_018659.2:c.397G>C NP_061129.1:p.Asp133His
XR_925085.1:n.149-4758C>G
XR_925086.1:n.149-4758C>G
XR_925087.1:n.149-4758C>G
XM_017008299.1:c.*47G>C XP_016863788.1:n.*47G>C
NM_018659.3:c.397G>C MANE Select NP_061129.1:p.Asp133His