Canonical Allele Identifier: CA1419338085

Gene: MECOM

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169198452T= , CM000665.2:g.169198452T=	GRCh38
NC_000003.11:g.168916240T= , CM000665.1:g.168916240T=	GRCh37
NC_000003.10:g.170398934T=	NCBI36
NG_028279.1:g.470324A=
NG_028279.2:g.470324A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494292.6:c.376-54620A=	ENSP00000417899.1:n.376-54620A=
ENST00000651503.2:c.376-54620A= MANE Select	ENSP00000498411.1:n.376-54620A=
ENST00000481315.1:c.-189-54620A=	ENSP00000418046.1:n.-189-54620A=
ENST00000485957.1:n.622-48697A=
ENST00000494292.5:c.376-54620A=	ENSP00000417899.1:n.376-54620A=
NM_001205194.1:c.-189-54620A=	NP_001192123.1:n.-189-54620A=
NM_004991.3:c.376-54620A=	NP_004982.2:n.376-54620A=
XM_005247213.2:c.376-54620A=	XP_005247270.1:n.376-54620A=
XM_005247214.2:c.376-54620A=	XP_005247271.1:n.376-54620A=
XM_005247215.2:c.376-54620A=	XP_005247272.1:n.376-54620A=
XM_005247224.2:c.376-54620A=	XP_005247281.1:n.376-54620A=
XM_005247225.2:c.376-54620A=	XP_005247282.1:n.376-54620A=
XM_005247226.2:c.376-54620A=	XP_005247283.1:n.376-54620A=
XM_011512546.1:c.28-54620A=	XP_011510848.1:n.28-54620A=
XR_924697.1:n.168+6472T=
NM_001366466.1:c.376-54620A=	NP_001353395.1:n.376-54620A=
NM_001366473.1:c.376-54620A=	NP_001353402.1:n.376-54620A=
XM_005247213.3:c.376-54620A=	XP_005247270.1:n.376-54620A=
XM_005247214.3:c.376-54620A=	XP_005247271.1:n.376-54620A=
XM_005247224.3:c.376-54620A=	XP_005247281.1:n.376-54620A=
XM_005247225.4:c.376-54620A=	XP_005247282.1:n.376-54620A=
XM_011512546.2:c.28-54620A=	XP_011510848.1:n.28-54620A=
XM_017005877.1:c.376-54620A=	XP_016861366.1:n.376-54620A=
NM_001205194.2:c.-189-54620A=	NP_001192123.1:n.-189-54620A=
NM_001366466.2:c.376-54620A=	NP_001353395.1:n.376-54620A=
NM_001366473.2:c.376-54620A=	NP_001353402.1:n.376-54620A=
NM_004991.4:c.376-54620A= MANE Select	NP_004982.2:n.376-54620A=