Canonical Allele Identifier: CA833588927

Gene: EXOC4

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.133650423T>C , CM000669.2:g.133650423T>C	GRCh38
NC_000007.13:g.133335176T>C , CM000669.1:g.133335176T>C	GRCh37
NC_000007.12:g.132985716T>C	NCBI36
NG_047176.1:g.402357T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253861.5:c.1514+20282T>C MANE Select	ENSP00000253861.4:n.1514+20282T>C
ENST00000253861.4:c.1514+20282T>C	ENSP00000253861.4:n.1514+20282T>C
ENST00000460346.5:n.270+20282T>C
ENST00000469115.5:n.397+20282T>C
ENST00000479839.6:n.402+20282T>C
ENST00000482089.5:n.270+20282T>C
ENST00000483800.5:n.251+20282T>C
ENST00000489931.5:n.270+20282T>C
NM_021807.3:c.1514+20282T>C	NP_068579.3:n.1514+20282T>C
XM_017012494.2:c.344+20282T>C	XP_016867983.1:n.344+20282T>C
XR_001744845.2:n.1541+20282T>C
NM_021807.4:c.1514+20282T>C MANE Select	NP_068579.3:n.1514+20282T>C