Canonical Allele Identifier: CA478521227

Gene: EMG1

Linked Data

• MyVariant Identifiers: chr12:g.7083587A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6974425A>T , CM000674.2:g.6974425A>T	GRCh38
NC_000012.11:g.7083587A>T , CM000674.1:g.7083587A>T	GRCh37
NC_000012.10:g.6953848A>T	NCBI36
NG_021408.1:g.8645A>T
NG_021408.2:g.8645A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599672.6:c.255A>T MANE Select	ENSP00000470560.1:p.Pro85=
ENST00000261406.7:c.237A>T	ENSP00000476966.2:p.Pro79=
ENST00000539196.2:c.118A>T
ENST00000599672.5:c.255A>T	ENSP00000470560.1:p.Pro85=
ENST00000607161.5:c.258A>T	ENSP00000480420.1:p.Pro86=
ENST00000611981.1:n.266A>T
ENST00000620255.1:n.244A>T
NM_006331.7:c.255A>T	NP_006322.4:p.Pro85=
XM_011520907.1:c.255A>T	XP_011519209.1:p.Pro85=
NM_001320049.1:c.255A>T	NP_001306978.1:p.Pro85=
NR_135131.1:n.398A>T
NM_006331.8:c.255A>T MANE Select	NP_006322.4:p.Pro85=
NM_001320049.2:c.255A>T	NP_001306978.1:p.Pro85=
NR_135131.2:n.266A>T