Canonical Allele Identifier: CA2302923156

Gene: ME2

Linked Data

• dbSNP Id: rs1917853850

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.50937880_50937881insGCG , CM000680.2:g.50937880_50937881insGCG	GRCh38
NC_000018.9:g.48464250_48464251insGCG , CM000680.1:g.48464250_48464251insGCG	GRCh37
NC_000018.8:g.46718248_46718249insGCG	NCBI36
NG_016198.1:g.63819_63820insGCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321341.11:c.1418-1690_1418-1689insGCG MANE Select	ENSP00000321070.5:n.1418-1690_1418-1689insGCG
ENST00000585680.2:c.1108-2408_1108-2407insGCG	ENSP00000491793.1:n.1108-2408_1108-2407insGCG
ENST00000638410.1:c.1418-1690_1418-1689insGCG	ENSP00000492272.1:n.1418-1690_1418-1689insGCG
ENST00000638937.1:c.1418-1690_1418-1689insGCG	ENSP00000492393.1:n.1418-1690_1418-1689insGCG
ENST00000639115.1:c.*940-1690_*940-1689insGCG	ENSP00000492733.1:n.*940-1690_*940-1689insGCG
ENST00000639255.1:c.1256-1690_1256-1689insGCG	ENSP00000492085.1:n.1256-1690_1256-1689insGCG
ENST00000639398.1:c.*778-1690_*778-1689insGCG	ENSP00000492309.1:n.*778-1690_*778-1689insGCG
ENST00000639612.1:c.1176-2408_1176-2407insGCG
ENST00000639665.1:c.1307-2408_1307-2407insGCG	ENSP00000491520.1:n.1307-2408_1307-2407insGCG
ENST00000639850.1:c.1304-1690_1304-1689insGCG	ENSP00000491152.1:n.1304-1690_1304-1689insGCG
ENST00000640530.1:c.*778-1690_*778-1689insGCG	ENSP00000491724.1:n.*778-1690_*778-1689insGCG
ENST00000640965.1:c.1307-1690_1307-1689insGCG	ENSP00000491954.1:n.1307-1690_1307-1689insGCG
ENST00000640967.1:c.1418-2408_1418-2407insGCG	ENSP00000492067.1:n.1418-2408_1418-2407insGCG
ENST00000321341.9:c.1418-1690_1418-1689insGCG	ENSP00000321070.5:n.1418-1690_1418-1689insGCG
ENST00000382927.3:c.1417+5520_1417+5521insGCG	ENSP00000372384.2:n.1417+5520_1417+5521insGCG
ENST00000585680.1:n.143-2408_143-2407insGCG
NM_001168335.1:c.1417+5520_1417+5521insGCG	NP_001161807.1:n.1417+5520_1417+5521insGCG
NM_002396.4:c.1418-1690_1418-1689insGCG	NP_002387.1:n.1418-1690_1418-1689insGCG
XR_935223.1:n.2135-2408_2135-2407insGCG
XR_935223.2:n.2037-2408_2037-2407insGCG
NM_002396.5:c.1418-1690_1418-1689insGCG MANE Select	NP_002387.1:n.1418-1690_1418-1689insGCG
NM_001168335.2:c.1417+5520_1417+5521insGCG	NP_001161807.1:n.1417+5520_1417+5521insGCG
NR_174094.1:n.1621-2408_1621-2407insGCG