Canonical Allele Identifier: CA2014342594

Gene: EMG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6974465_6974466delinsAC , CM000674.2:g.6974465_6974466delinsAC	GRCh38
NC_000012.11:g.7083627_7083628delinsAC , CM000674.1:g.7083627_7083628delinsAC	GRCh37
NC_000012.10:g.6953888_6953889delinsAC	NCBI36
NG_021408.1:g.8685_8686delinsAC
NG_021408.2:g.8685_8686delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599672.6:c.270+25_270+26delinsAC MANE Select	ENSP00000470560.1:n.270+25_270+26delinsAC
ENST00000261406.7:c.252+25_252+26delinsAC	ENSP00000476966.2:n.252+25_252+26delinsAC
ENST00000539196.2:c.133+25_133+26delinsAC
ENST00000599672.5:c.270+25_270+26delinsAC	ENSP00000470560.1:n.270+25_270+26delinsAC
ENST00000607161.5:c.273+25_273+26delinsAC	ENSP00000480420.1:n.273+25_273+26delinsAC
ENST00000611981.1:n.281+25_281+26delinsAC
ENST00000620255.1:n.284_285delinsAC
NM_006331.7:c.270+25_270+26delinsAC	NP_006322.4:n.270+25_270+26delinsAC
XM_011520907.1:c.270+25_270+26delinsAC	XP_011519209.1:n.270+25_270+26delinsAC
NM_001320049.1:c.270+25_270+26delinsAC	NP_001306978.1:n.270+25_270+26delinsAC
NR_135131.1:n.413+25_413+26delinsAC
NM_006331.8:c.270+25_270+26delinsAC MANE Select	NP_006322.4:n.270+25_270+26delinsAC
NM_001320049.2:c.270+25_270+26delinsAC	NP_001306978.1:n.270+25_270+26delinsAC
NR_135131.2:n.281+25_281+26delinsAC