Canonical Allele Identifier: CA2617379579

Gene: EMG1

Linked Data

• gnomAD v4: 12-6974508-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6974508C>A , CM000674.2:g.6974508C>A	GRCh38
NC_000012.11:g.7083670C>A , CM000674.1:g.7083670C>A	GRCh37
NC_000012.10:g.6953931C>A	NCBI36
NG_021408.1:g.8728C>A
NG_021408.2:g.8728C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599672.6:c.271-44C>A MANE Select	ENSP00000470560.1:n.271-44C>A
ENST00000261406.7:c.253-44C>A	ENSP00000476966.2:n.253-44C>A
ENST00000539196.2:c.134-44C>A
ENST00000599672.5:c.271-44C>A	ENSP00000470560.1:n.271-44C>A
ENST00000607161.5:c.274-44C>A	ENSP00000480420.1:n.274-44C>A
ENST00000611981.1:n.282-44C>A
ENST00000620255.1:n.327C>A
NM_006331.7:c.271-44C>A	NP_006322.4:n.271-44C>A
XM_011520907.1:c.271-44C>A	XP_011519209.1:n.271-44C>A
NM_001320049.1:c.271-44C>A	NP_001306978.1:n.271-44C>A
NR_135131.1:n.414-44C>A
NM_006331.8:c.271-44C>A MANE Select	NP_006322.4:n.271-44C>A
NM_001320049.2:c.271-44C>A	NP_001306978.1:n.271-44C>A
NR_135131.2:n.282-44C>A