Canonical Allele Identifier: CA2014342535

Gene: EMG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6974327_6974329delinsCCT , CM000674.2:g.6974327_6974329delinsCCT	GRCh38
NC_000012.11:g.7083489_7083491delinsCCT , CM000674.1:g.7083489_7083491delinsCCT	GRCh37
NC_000012.10:g.6953750_6953752delinsCCT	NCBI36
NG_021408.1:g.8547_8549delinsCCT
NG_021408.2:g.8547_8549delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599672.6:c.169-12_169-10delinsCCT MANE Select	ENSP00000470560.1:n.169-12_169-10delinsCCT
ENST00000261406.7:c.151-12_151-10delinsCCT	ENSP00000476966.2:n.151-12_151-10delinsCCT
ENST00000539196.2:c.32-12_32-10delinsCCT
ENST00000599672.5:c.169-12_169-10delinsCCT	ENSP00000470560.1:n.169-12_169-10delinsCCT
ENST00000607161.5:c.172-12_172-10delinsCCT	ENSP00000480420.1:n.172-12_172-10delinsCCT
ENST00000611981.1:n.180-12_180-10delinsCCT
ENST00000620255.1:n.158-12_158-10delinsCCT
NM_006331.7:c.169-12_169-10delinsCCT	NP_006322.4:n.169-12_169-10delinsCCT
XM_011520907.1:c.169-12_169-10delinsCCT	XP_011519209.1:n.169-12_169-10delinsCCT
NM_001320049.1:c.169-12_169-10delinsCCT	NP_001306978.1:n.169-12_169-10delinsCCT
NR_135131.1:n.312-12_312-10delinsCCT
NM_006331.8:c.169-12_169-10delinsCCT MANE Select	NP_006322.4:n.169-12_169-10delinsCCT
NM_001320049.2:c.169-12_169-10delinsCCT	NP_001306978.1:n.169-12_169-10delinsCCT
NR_135131.2:n.180-12_180-10delinsCCT