Canonical Allele Identifier: CA87781303

Gene: ECT2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.172758629G>A , CM000665.2:g.172758629G>A	GRCh38
NC_000003.11:g.172476419G>A , CM000665.1:g.172476419G>A	GRCh37
NC_000003.10:g.173959113G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392692.8:c.487-351G>A MANE Select	ENSP00000376457.3:n.487-351G>A
ENST00000232458.9:c.394-351G>A	ENSP00000232458.5:n.394-351G>A
ENST00000392692.7:c.487-351G>A	ENSP00000376457.3:n.487-351G>A
ENST00000415665.5:c.394-351G>A	ENSP00000412028.1:n.394-351G>A
ENST00000417960.5:c.391-351G>A	ENSP00000415876.1:n.391-351G>A
ENST00000428567.5:c.391-351G>A	ENSP00000403501.1:n.391-351G>A
ENST00000441497.6:c.394-351G>A	ENSP00000412259.2:n.394-351G>A
ENST00000540509.5:c.394-351G>A	ENSP00000443160.2:n.394-351G>A
NM_001258315.1:c.487-351G>A	NP_001245244.1:n.487-351G>A
NM_001258316.1:c.394-351G>A	NP_001245245.1:n.394-351G>A
NM_018098.5:c.394-351G>A	NP_060568.3:n.394-351G>A
XM_005247176.1:c.394-351G>A	XP_005247233.1:n.394-351G>A
XM_006713523.2:c.487-351G>A	XP_006713586.1:n.487-351G>A
XM_006713524.2:c.487-351G>A	XP_006713587.1:n.487-351G>A
XM_011512514.1:c.487-351G>A	XP_011510816.1:n.487-351G>A
XM_011512515.1:c.487-351G>A	XP_011510817.1:n.487-351G>A
XM_011512516.1:c.394-351G>A	XP_011510818.1:n.394-351G>A
NM_001349094.1:c.487-351G>A	NP_001336023.1:n.487-351G>A
NM_001349095.1:c.487-351G>A	NP_001336024.1:n.487-351G>A
NM_001349096.1:c.487-351G>A	NP_001336025.1:n.487-351G>A
NM_001349097.1:c.484-351G>A	NP_001336026.1:n.484-351G>A
NM_001349098.1:c.487-351G>A	NP_001336027.1:n.487-351G>A
NM_001349099.1:c.487-351G>A	NP_001336028.1:n.487-351G>A
NM_001349100.1:c.487-351G>A	NP_001336029.1:n.487-351G>A
NM_001349101.1:c.394-351G>A	NP_001336030.1:n.394-351G>A
NM_001349102.1:c.391-351G>A	NP_001336031.1:n.391-351G>A
NM_001349103.1:c.394-351G>A	NP_001336032.1:n.394-351G>A
NM_001349104.1:c.394-351G>A	NP_001336033.1:n.394-351G>A
XM_005247176.2:c.394-351G>A	XP_005247233.1:n.394-351G>A
XM_006713524.4:c.487-351G>A	XP_006713587.1:n.487-351G>A
XM_011512514.2:c.487-351G>A	XP_011510816.1:n.487-351G>A
XM_017005831.1:c.487-351G>A	XP_016861320.1:n.487-351G>A
XM_017005832.1:c.394-351G>A	XP_016861321.1:n.394-351G>A
NM_001258315.2:c.487-351G>A MANE Select	NP_001245244.1:n.487-351G>A
NM_001349094.2:c.487-351G>A	NP_001336023.1:n.487-351G>A
NM_001349095.2:c.487-351G>A	NP_001336024.1:n.487-351G>A
NM_001349096.2:c.487-351G>A	NP_001336025.1:n.487-351G>A
NM_001349097.2:c.484-351G>A	NP_001336026.1:n.484-351G>A
NM_001349098.2:c.487-351G>A	NP_001336027.1:n.487-351G>A
NM_001349099.2:c.487-351G>A	NP_001336028.1:n.487-351G>A
NM_001349100.2:c.487-351G>A	NP_001336029.1:n.487-351G>A
NM_001349101.2:c.394-351G>A	NP_001336030.1:n.394-351G>A
NM_001349102.2:c.391-351G>A	NP_001336031.1:n.391-351G>A
NM_001349103.2:c.394-351G>A	NP_001336032.1:n.394-351G>A
NM_001349104.2:c.394-351G>A	NP_001336033.1:n.394-351G>A
NM_018098.6:c.394-351G>A	NP_060568.3:n.394-351G>A
NM_001258316.2:c.394-351G>A	NP_001245245.1:n.394-351G>A