Canonical Allele Identifier: CA654081738

Gene: EMG1

Linked Data

• COSMIC: COSN4703727 ; COSN22512683

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6974500G>A , CM000674.2:g.6974500G>A	GRCh38
NC_000012.11:g.7083662G>A , CM000674.1:g.7083662G>A	GRCh37
NC_000012.10:g.6953923G>A	NCBI36
NG_021408.1:g.8720G>A
NG_021408.2:g.8720G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599672.6:c.271-52G>A MANE Select	ENSP00000470560.1:n.271-52G>A
ENST00000261406.7:c.253-52G>A	ENSP00000476966.2:n.253-52G>A
ENST00000539196.2:c.134-52G>A
ENST00000599672.5:c.271-52G>A	ENSP00000470560.1:n.271-52G>A
ENST00000607161.5:c.274-52G>A	ENSP00000480420.1:n.274-52G>A
ENST00000611981.1:n.282-52G>A
ENST00000620255.1:n.319G>A
NM_006331.7:c.271-52G>A	NP_006322.4:n.271-52G>A
XM_011520907.1:c.271-52G>A	XP_011519209.1:n.271-52G>A
NM_001320049.1:c.271-52G>A	NP_001306978.1:n.271-52G>A
NR_135131.1:n.414-52G>A
NM_006331.8:c.271-52G>A MANE Select	NP_006322.4:n.271-52G>A
NM_001320049.2:c.271-52G>A	NP_001306978.1:n.271-52G>A
NR_135131.2:n.282-52G>A