Canonical Allele Identifier: CA383683149

Gene: EMG1

Linked Data

• gnomAD v4: 12-6974436-A-G
• MyVariant Identifiers: chr12:g.7083598A>G (hg19) ; chr12:g.6974436A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6974436A>G , CM000674.2:g.6974436A>G	GRCh38
NC_000012.11:g.7083598A>G , CM000674.1:g.7083598A>G	GRCh37
NC_000012.10:g.6953859A>G	NCBI36
NG_021408.1:g.8656A>G
NG_021408.2:g.8656A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000599672.6:c.266A>G MANE Select	ENSP00000470560.1:p.His89Arg
ENST00000261406.7:c.248A>G	ENSP00000476966.2:p.His83Arg
ENST00000539196.2:c.129A>G
ENST00000599672.5:c.266A>G	ENSP00000470560.1:p.His89Arg
ENST00000607161.5:c.269A>G	ENSP00000480420.1:p.His90Arg
ENST00000611981.1:n.277A>G
ENST00000620255.1:n.255A>G
NM_006331.7:c.266A>G	NP_006322.4:p.His89Arg
XM_011520907.1:c.266A>G	XP_011519209.1:p.His89Arg
NM_001320049.1:c.266A>G	NP_001306978.1:p.His89Arg
NR_135131.1:n.409A>G
NM_006331.8:c.266A>G MANE Select	NP_006322.4:p.His89Arg
NM_001320049.2:c.266A>G	NP_001306978.1:p.His89Arg
NR_135131.2:n.277A>G