Canonical Allele Identifier: CA902364082

Gene: MECOM

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169383111G>C , CM000665.2:g.169383111G>C	GRCh38
NC_000003.11:g.169100899G>C , CM000665.1:g.169100899G>C	GRCh37
NC_000003.10:g.170583593G>C	NCBI36
NG_028279.1:g.285665C>G
NG_028279.2:g.285665C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486748.2:c.110-1587C>G	ENSP00000419537.1:n.110-1587C>G
ENST00000494292.6:c.38-1587C>G	ENSP00000417899.1:n.38-1587C>G
ENST00000651503.2:c.38-1587C>G MANE Select	ENSP00000498411.1:n.38-1587C>G
ENST00000485957.1:n.284-1587C>G
ENST00000486748.1:c.110-1587C>G	ENSP00000419537.1:n.110-1587C>G
ENST00000494292.5:c.38-1587C>G	ENSP00000417899.1:n.38-1587C>G
NM_001205194.1:c.-189-239279C>G	NP_001192123.1:n.-189-239279C>G
NM_004991.3:c.38-1587C>G	NP_004982.2:n.38-1587C>G
XM_005247213.2:c.38-1587C>G	XP_005247270.1:n.38-1587C>G
XM_005247214.2:c.38-1587C>G	XP_005247271.1:n.38-1587C>G
XM_005247215.2:c.38-1587C>G	XP_005247272.1:n.38-1587C>G
XM_005247224.2:c.38-1587C>G	XP_005247281.1:n.38-1587C>G
XM_005247225.2:c.38-1587C>G	XP_005247282.1:n.38-1587C>G
XM_005247226.2:c.38-1587C>G	XP_005247283.1:n.38-1587C>G
NM_001366466.1:c.38-1587C>G	NP_001353395.1:n.38-1587C>G
NM_001366473.1:c.38-1587C>G	NP_001353402.1:n.38-1587C>G
XM_005247213.3:c.38-1587C>G	XP_005247270.1:n.38-1587C>G
XM_005247214.3:c.38-1587C>G	XP_005247271.1:n.38-1587C>G
XM_005247224.3:c.38-1587C>G	XP_005247281.1:n.38-1587C>G
XM_005247225.4:c.38-1587C>G	XP_005247282.1:n.38-1587C>G
XM_017005877.1:c.38-1587C>G	XP_016861366.1:n.38-1587C>G
NM_001205194.2:c.-189-239279C>G	NP_001192123.1:n.-189-239279C>G
NM_001366466.2:c.38-1587C>G	NP_001353395.1:n.38-1587C>G
NM_001366473.2:c.38-1587C>G	NP_001353402.1:n.38-1587C>G
NM_004991.4:c.38-1587C>G MANE Select	NP_004982.2:n.38-1587C>G