Canonical Allele Identifier: CA2302923145

Gene: ME2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.50937852T= , CM000680.2:g.50937852T=	GRCh38
NC_000018.9:g.48464222T= , CM000680.1:g.48464222T=	GRCh37
NC_000018.8:g.46718220T=	NCBI36
NG_016198.1:g.63791T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321341.11:c.1418-1718T= MANE Select	ENSP00000321070.5:n.1418-1718T=
ENST00000585680.2:c.1108-2436T=	ENSP00000491793.1:n.1108-2436T=
ENST00000638410.1:c.1418-1718T=	ENSP00000492272.1:n.1418-1718T=
ENST00000638937.1:c.1418-1718T=	ENSP00000492393.1:n.1418-1718T=
ENST00000639115.1:c.*940-1718T=	ENSP00000492733.1:n.*940-1718T=
ENST00000639255.1:c.1256-1718T=	ENSP00000492085.1:n.1256-1718T=
ENST00000639398.1:c.*778-1718T=	ENSP00000492309.1:n.*778-1718T=
ENST00000639612.1:c.1176-2436T=
ENST00000639665.1:c.1307-2436T=	ENSP00000491520.1:n.1307-2436T=
ENST00000639850.1:c.1304-1718T=	ENSP00000491152.1:n.1304-1718T=
ENST00000640530.1:c.*778-1718T=	ENSP00000491724.1:n.*778-1718T=
ENST00000640965.1:c.1307-1718T=	ENSP00000491954.1:n.1307-1718T=
ENST00000640967.1:c.1418-2436T=	ENSP00000492067.1:n.1418-2436T=
ENST00000321341.9:c.1418-1718T=	ENSP00000321070.5:n.1418-1718T=
ENST00000382927.3:c.1417+5492T=	ENSP00000372384.2:n.1417+5492T=
ENST00000585680.1:n.143-2436T=
NM_001168335.1:c.1417+5492T=	NP_001161807.1:n.1417+5492T=
NM_002396.4:c.1418-1718T=	NP_002387.1:n.1418-1718T=
XR_935223.1:n.2135-2436T=
XR_935223.2:n.2037-2436T=
NM_002396.5:c.1418-1718T= MANE Select	NP_002387.1:n.1418-1718T=
NM_001168335.2:c.1417+5492T=	NP_001161807.1:n.1417+5492T=
NR_174094.1:n.1621-2436T=