Canonical Allele Identifier: CA356273412

Gene: CYTL1

Linked Data

• MyVariant Identifiers: chr4:g.5016886G>T (hg19) ; chr4:g.5015159G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307746.9:c.403C>A MANE Select	ENSP00000303550.4:p.Gln135Lys
ENST00000307746.8:c.403C>A	ENSP00000303550.4:p.Gln135Lys
ENST00000506508.1:c.221C>A
ENST00000509419.1:c.270C>A
NM_018659.2:c.403C>A	NP_061129.1:p.Gln135Lys
XR_925085.1:n.149-4764G>T
XR_925086.1:n.149-4764G>T
XR_925087.1:n.149-4764G>T
XM_017008299.1:c.*53C>A	XP_016863788.1:n.*53C>A
NM_018659.3:c.403C>A MANE Select	NP_061129.1:p.Gln135Lys