Canonical Allele Identifier: CA167488935

Gene: EXOC4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.134063193G>C , CM000669.2:g.134063193G>C	GRCh38
NC_000007.13:g.133747946G>C , CM000669.1:g.133747946G>C	GRCh37
NC_000007.12:g.133398486G>C	NCBI36
NG_047176.1:g.815127G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253861.5:c.2688-1098G>C MANE Select	ENSP00000253861.4:n.2688-1098G>C
ENST00000253861.4:c.2688-1098G>C	ENSP00000253861.4:n.2688-1098G>C
ENST00000459626.1:n.425-1098G>C
ENST00000466000.1:n.236-1098G>C
NM_021807.3:c.2688-1098G>C	NP_068579.3:n.2688-1098G>C
XM_017012494.2:c.1518-1098G>C	XP_016867983.1:n.1518-1098G>C
XR_001744845.2:n.2715-1098G>C
NM_021807.4:c.2688-1098G>C MANE Select	NP_068579.3:n.2688-1098G>C