Canonical Allele Identifier: CA1419469367

Gene: MECOM MECOM-AS1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169448100C>G , CM000665.2:g.169448100C>G	GRCh38
NC_000003.11:g.169165888C>G , CM000665.1:g.169165888C>G	GRCh37
NC_000003.10:g.170648582C>G	NCBI36
NG_028279.1:g.220676G>C
NG_028279.2:g.220676G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486748.2:c.110-66576G>C (MECOM)	ENSP00000419537.1:n.110-66576G>C
ENST00000494292.6:c.38-66576G>C (MECOM)	ENSP00000417899.1:n.38-66576G>C
ENST00000651503.2:c.38-66576G>C (MECOM) MANE Select	ENSP00000498411.1:n.38-66576G>C
ENST00000485957.1:n.284-66576G>C (MECOM)
ENST00000486748.1:c.110-66576G>C (MECOM)	ENSP00000419537.1:n.110-66576G>C
ENST00000494292.5:c.38-66576G>C (MECOM)	ENSP00000417899.1:n.38-66576G>C
NM_001205194.1:c.-190+215236G>C (MECOM)	NP_001192123.1:n.-190+215236G>C
NM_004991.3:c.38-66576G>C (MECOM)	NP_004982.2:n.38-66576G>C
XM_005247213.2:c.38-66576G>C (MECOM)	XP_005247270.1:n.38-66576G>C
XM_005247214.2:c.38-66576G>C (MECOM)	XP_005247271.1:n.38-66576G>C
XM_005247215.2:c.38-66576G>C (MECOM)	XP_005247272.1:n.38-66576G>C
XM_005247224.2:c.38-66576G>C (MECOM)	XP_005247281.1:n.38-66576G>C
XM_005247225.2:c.38-66576G>C (MECOM)	XP_005247282.1:n.38-66576G>C
XM_005247226.2:c.38-66576G>C (MECOM)	XP_005247283.1:n.38-66576G>C
XR_924693.1:n.161+165C>G (MECOM-AS1)
XR_924694.1:n.161+165C>G (MECOM-AS1)
XR_924695.1:n.97+229C>G (MECOM-AS1)
NM_001366466.1:c.38-66576G>C (MECOM)	NP_001353395.1:n.38-66576G>C
NM_001366473.1:c.38-66576G>C (MECOM)	NP_001353402.1:n.38-66576G>C
NR_134932.1:n.69+165C>G (MECOM-AS1)
XM_005247213.3:c.38-66576G>C (MECOM)	XP_005247270.1:n.38-66576G>C
XM_005247214.3:c.38-66576G>C (MECOM)	XP_005247271.1:n.38-66576G>C
XM_005247224.3:c.38-66576G>C (MECOM)	XP_005247281.1:n.38-66576G>C
XM_005247225.4:c.38-66576G>C (MECOM)	XP_005247282.1:n.38-66576G>C
XM_017005877.1:c.38-66576G>C (MECOM)	XP_016861366.1:n.38-66576G>C
NM_001205194.2:c.-190+215236G>C (MECOM)	NP_001192123.1:n.-190+215236G>C
NM_001366466.2:c.38-66576G>C (MECOM)	NP_001353395.1:n.38-66576G>C
NM_001366473.2:c.38-66576G>C (MECOM)	NP_001353402.1:n.38-66576G>C
NM_004991.4:c.38-66576G>C (MECOM) MANE Select	NP_004982.2:n.38-66576G>C