Canonical Allele Identifier: CA383683332

Gene: EMG1

Linked Data

• MyVariant Identifiers: chr12:g.7083716T>G (hg19) ; chr12:g.6974554T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6974554T>G , CM000674.2:g.6974554T>G	GRCh38
NC_000012.11:g.7083716T>G , CM000674.1:g.7083716T>G	GRCh37
NC_000012.10:g.6953977T>G	NCBI36
NG_021408.1:g.8774T>G
NG_021408.2:g.8774T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599672.6:c.273T>G MANE Select	ENSP00000470560.1:p.Ser91Arg
ENST00000261406.7:c.255T>G	ENSP00000476966.2:p.Ser85Arg
ENST00000539196.2:c.136T>G
ENST00000599672.5:c.273T>G	ENSP00000470560.1:p.Ser91Arg
ENST00000607161.5:c.276T>G	ENSP00000480420.1:p.Ser92Arg
ENST00000611981.1:n.284T>G
ENST00000620255.1:n.373T>G
NM_006331.7:c.273T>G	NP_006322.4:p.Ser91Arg
XM_011520907.1:c.273T>G	XP_011519209.1:p.Ser91Arg
NM_001320049.1:c.273T>G	NP_001306978.1:p.Ser91Arg
NR_135131.1:n.416T>G
NM_006331.8:c.273T>G MANE Select	NP_006322.4:p.Ser91Arg
NM_001320049.2:c.273T>G	NP_001306978.1:p.Ser91Arg
NR_135131.2:n.284T>G