Canonical Allele Identifier: CA2014342629

Gene: EMG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6974511C= , CM000674.2:g.6974511C=	GRCh38
NC_000012.11:g.7083673C= , CM000674.1:g.7083673C=	GRCh37
NC_000012.10:g.6953934C=	NCBI36
NG_021408.1:g.8731C=
NG_021408.2:g.8731C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599672.6:c.271-41C= MANE Select	ENSP00000470560.1:n.271-41C=
ENST00000261406.7:c.253-41C=	ENSP00000476966.2:n.253-41C=
ENST00000539196.2:c.134-41C=
ENST00000599672.5:c.271-41C=	ENSP00000470560.1:n.271-41C=
ENST00000607161.5:c.274-41C=	ENSP00000480420.1:n.274-41C=
ENST00000611981.1:n.282-41C=
ENST00000620255.1:n.330C=
NM_006331.7:c.271-41C=	NP_006322.4:n.271-41C=
XM_011520907.1:c.271-41C=	XP_011519209.1:n.271-41C=
NM_001320049.1:c.271-41C=	NP_001306978.1:n.271-41C=
NR_135131.1:n.414-41C=
NM_006331.8:c.271-41C= MANE Select	NP_006322.4:n.271-41C=
NM_001320049.2:c.271-41C=	NP_001306978.1:n.271-41C=
NR_135131.2:n.282-41C=