Canonical Allele Identifier: CA383682530

Gene: EMG1

Linked Data

• MyVariant Identifiers: chr12:g.7083520T>A (hg19) ; chr12:g.6974358T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6974358T>A , CM000674.2:g.6974358T>A	GRCh38
NC_000012.11:g.7083520T>A , CM000674.1:g.7083520T>A	GRCh37
NC_000012.10:g.6953781T>A	NCBI36
NG_021408.1:g.8578T>A
NG_021408.2:g.8578T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000599672.6:c.188T>A MANE Select	ENSP00000470560.1:p.Leu63Gln
ENST00000261406.7:c.170T>A	ENSP00000476966.2:p.Leu57Gln
ENST00000539196.2:c.51T>A
ENST00000599672.5:c.188T>A	ENSP00000470560.1:p.Leu63Gln
ENST00000607161.5:c.191T>A	ENSP00000480420.1:p.Leu64Gln
ENST00000611981.1:n.199T>A
ENST00000620255.1:n.177T>A
NM_006331.7:c.188T>A	NP_006322.4:p.Leu63Gln
XM_011520907.1:c.188T>A	XP_011519209.1:p.Leu63Gln
NM_001320049.1:c.188T>A	NP_001306978.1:p.Leu63Gln
NR_135131.1:n.331T>A
NM_006331.8:c.188T>A MANE Select	NP_006322.4:p.Leu63Gln
NM_001320049.2:c.188T>A	NP_001306978.1:p.Leu63Gln
NR_135131.2:n.199T>A