Canonical Allele Identifier: CA356273406

Gene: CYTL1

Linked Data

• MyVariant Identifiers: chr4:g.5016883G>T (hg19) ; chr4:g.5015156G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5015156G>T , CM000666.2:g.5015156G>T	GRCh38
NC_000004.11:g.5016883G>T , CM000666.1:g.5016883G>T	GRCh37
NC_000004.10:g.5067784G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000307746.9:c.406C>A MANE Select	ENSP00000303550.4:p.Arg136Ser
ENST00000307746.8:c.406C>A	ENSP00000303550.4:p.Arg136Ser
ENST00000506508.1:c.224C>A
ENST00000509419.1:c.273C>A
NM_018659.2:c.406C>A	NP_061129.1:p.Arg136Ser
XR_925085.1:n.149-4767G>T
XR_925086.1:n.149-4767G>T
XR_925087.1:n.149-4767G>T
XM_017008299.1:c.*56C>A	XP_016863788.1:n.*56C>A
NM_018659.3:c.406C>A MANE Select	NP_061129.1:p.Arg136Ser