Canonical Allele Identifier: CA14926694

Gene: CYTH4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.37283446C>G , CM000684.2:g.37283446C>G	GRCh38
NC_000022.10:g.37679487C>G , CM000684.1:g.37679487C>G	GRCh37
NC_000022.9:g.36009433C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248901.11:c.19+858C>G MANE Select	ENSP00000248901.6:n.19+858C>G
ENST00000248901.10:c.19+858C>G	ENSP00000248901.6:n.19+858C>G
ENST00000402997.5:c.19+858C>G	ENSP00000385997.1:n.19+858C>G
ENST00000405206.3:c.19+858C>G	ENSP00000384280.3:n.19+858C>G
ENST00000439667.1:n.58+858C>G
ENST00000457992.5:c.19+858C>G	ENSP00000405442.1:n.19+858C>G
ENST00000462927.5:n.64+858C>G
ENST00000469886.5:n.74+858C>G
ENST00000480510.5:n.62+858C>G
NM_013385.3:c.19+858C>G	NP_037517.1:n.19+858C>G
XM_011530148.1:c.-646+858C>G	XP_011528450.1:n.-646+858C>G
XR_430406.2:n.135+858C>G
NM_001318024.1:c.-172+858C>G	NP_001304953.1:n.-172+858C>G
NM_013385.4:c.19+858C>G	NP_037517.1:n.19+858C>G
XM_011530148.2:c.-646+858C>G	XP_011528450.1:n.-646+858C>G
XR_001755214.2:n.116+858C>G
NM_013385.5:c.19+858C>G MANE Select	NP_037517.1:n.19+858C>G
NM_001318024.2:c.-172+858C>G	NP_001304953.1:n.-172+858C>G