Canonical Allele Identifier: CA2302904990

Gene: ME2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.50896615A= , CM000680.2:g.50896615A=	GRCh38
NC_000018.9:g.48422985A= , CM000680.1:g.48422985A=	GRCh37
NC_000018.8:g.46676983A=	NCBI36
NG_016198.1:g.22554A=

Transcript Alleles

HGVS	Amino-acid Change
NM_002396.5:c.108+687A= MANE Select	NP_002387.1:n.108+687A=
ENST00000321341.11:c.108+687A= MANE Select	ENSP00000321070.5:n.108+687A=
NM_001168335.1:c.108+687A=	NP_001161807.1:n.108+687A=
NM_001168335.2:c.108+687A=	NP_001161807.1:n.108+687A=
NM_002396.4:c.108+687A=	NP_002387.1:n.108+687A=
NR_174094.1:n.311+687A=
ENST00000321341.9:c.108+687A=	ENSP00000321070.5:n.108+687A=
ENST00000382927.3:c.108+687A=	ENSP00000372384.2:n.108+687A=
ENST00000638410.1:c.108+687A=	ENSP00000492272.1:n.108+687A=
ENST00000638768.1:n.82+687A=
ENST00000638937.1:c.108+687A=	ENSP00000492393.1:n.108+687A=
ENST00000639115.1:c.108+687A=	ENSP00000492733.1:n.108+687A=
ENST00000639255.1:c.108+687A=	ENSP00000492085.1:n.108+687A=
ENST00000639398.1:c.108+687A=	ENSP00000492309.1:n.108+687A=
ENST00000639612.1:c.104+687A=
ENST00000639665.1:c.-3-11448A=	ENSP00000491520.1:n.-3-11448A=
ENST00000639688.1:c.108+687A=	ENSP00000492377.1:n.108+687A=
ENST00000639850.1:c.108+687A=	ENSP00000491152.1:n.108+687A=
ENST00000640530.1:c.108+687A=	ENSP00000491724.1:n.108+687A=
ENST00000640965.1:c.-3-11448A=	ENSP00000491954.1:n.-3-11448A=
ENST00000640967.1:c.108+687A=	ENSP00000492067.1:n.108+687A=
XR_935223.1:n.825+687A=
XR_935223.2:n.727+687A=