Canonical Allele Identifier: CA1419391980
Gene: MECOM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169364775A= , CM000665.2:g.169364775A= GRCh38
NC_000003.11:g.169082563A= , CM000665.1:g.169082563A= GRCh37
NC_000003.10:g.170565257A= NCBI36
NG_028279.1:g.304001T=
NG_028279.2:g.304001T=

Transcript Alleles

HGVS Amino-acid change
ENST00000494292.6:c.375+16412T= ENSP00000417899.1:n.375+16412T=
ENST00000651503.2:c.375+16412T= MANE Select ENSP00000498411.1:n.375+16412T=
ENST00000485957.1:n.621+16412T=
ENST00000494292.5:c.375+16412T= ENSP00000417899.1:n.375+16412T=
NM_001205194.1:c.-189-220943T= NP_001192123.1:n.-189-220943T=
NM_004991.3:c.375+16412T= NP_004982.2:n.375+16412T=
XM_005247213.2:c.375+16412T= XP_005247270.1:n.375+16412T=
XM_005247214.2:c.375+16412T= XP_005247271.1:n.375+16412T=
XM_005247215.2:c.375+16412T= XP_005247272.1:n.375+16412T=
XM_005247224.2:c.375+16412T= XP_005247281.1:n.375+16412T=
XM_005247225.2:c.375+16412T= XP_005247282.1:n.375+16412T=
XM_005247226.2:c.375+16412T= XP_005247283.1:n.375+16412T=
NM_001366466.1:c.375+16412T= NP_001353395.1:n.375+16412T=
NM_001366473.1:c.375+16412T= NP_001353402.1:n.375+16412T=
XM_005247213.3:c.375+16412T= XP_005247270.1:n.375+16412T=
XM_005247214.3:c.375+16412T= XP_005247271.1:n.375+16412T=
XM_005247224.3:c.375+16412T= XP_005247281.1:n.375+16412T=
XM_005247225.4:c.375+16412T= XP_005247282.1:n.375+16412T=
XM_017005877.1:c.375+16412T= XP_016861366.1:n.375+16412T=
NM_001205194.2:c.-189-220943T= NP_001192123.1:n.-189-220943T=
NM_001366466.2:c.375+16412T= NP_001353395.1:n.375+16412T=
NM_001366473.2:c.375+16412T= NP_001353402.1:n.375+16412T=
NM_004991.4:c.375+16412T= MANE Select NP_004982.2:n.375+16412T=