Canonical Allele Identifier: CA356273413
Gene: CYTL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.5016886G>C (hg19) chr4:g.5015159G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.5015159G>C , CM000666.2:g.5015159G>C GRCh38
NC_000004.11:g.5016886G>C , CM000666.1:g.5016886G>C GRCh37
NC_000004.10:g.5067787G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000307746.9:c.403C>G MANE Select ENSP00000303550.4:p.Gln135Glu
ENST00000307746.8:c.403C>G ENSP00000303550.4:p.Gln135Glu
ENST00000506508.1:c.221C>G
ENST00000509419.1:c.270C>G
NM_018659.2:c.403C>G NP_061129.1:p.Gln135Glu
XR_925085.1:n.149-4764G>C
XR_925086.1:n.149-4764G>C
XR_925087.1:n.149-4764G>C
XM_017008299.1:c.*53C>G XP_016863788.1:n.*53C>G
NM_018659.3:c.403C>G MANE Select NP_061129.1:p.Gln135Glu
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