Canonical Allele Identifier: CA2014342627

Gene: EMG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6974508_6974510delinsCCT , CM000674.2:g.6974508_6974510delinsCCT	GRCh38
NC_000012.11:g.7083670_7083672delinsCCT , CM000674.1:g.7083670_7083672delinsCCT	GRCh37
NC_000012.10:g.6953931_6953933delinsCCT	NCBI36
NG_021408.1:g.8728_8730delinsCCT
NG_021408.2:g.8728_8730delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599672.6:c.271-44_271-42delinsCCT MANE Select	ENSP00000470560.1:n.271-44_271-42delinsCCT
ENST00000261406.7:c.253-44_253-42delinsCCT	ENSP00000476966.2:n.253-44_253-42delinsCCT
ENST00000539196.2:c.134-44_134-42delinsCCT
ENST00000599672.5:c.271-44_271-42delinsCCT	ENSP00000470560.1:n.271-44_271-42delinsCCT
ENST00000607161.5:c.274-44_274-42delinsCCT	ENSP00000480420.1:n.274-44_274-42delinsCCT
ENST00000611981.1:n.282-44_282-42delinsCCT
ENST00000620255.1:n.327_329delinsCCT
NM_006331.7:c.271-44_271-42delinsCCT	NP_006322.4:n.271-44_271-42delinsCCT
XM_011520907.1:c.271-44_271-42delinsCCT	XP_011519209.1:n.271-44_271-42delinsCCT
NM_001320049.1:c.271-44_271-42delinsCCT	NP_001306978.1:n.271-44_271-42delinsCCT
NR_135131.1:n.414-44_414-42delinsCCT
NM_006331.8:c.271-44_271-42delinsCCT MANE Select	NP_006322.4:n.271-44_271-42delinsCCT
NM_001320049.2:c.271-44_271-42delinsCCT	NP_001306978.1:n.271-44_271-42delinsCCT
NR_135131.2:n.282-44_282-42delinsCCT