Canonical Allele Identifier: CA2014342498

Gene: EMG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6974272T= , CM000674.2:g.6974272T=	GRCh38
NC_000012.11:g.7083434T= , CM000674.1:g.7083434T=	GRCh37
NC_000012.10:g.6953695T=	NCBI36
NG_021408.1:g.8492T=
NG_021408.2:g.8492T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599672.6:c.169-67T= MANE Select	ENSP00000470560.1:n.169-67T=
ENST00000261406.7:c.151-67T=	ENSP00000476966.2:n.151-67T=
ENST00000539196.2:c.32-67T=
ENST00000599672.5:c.169-67T=	ENSP00000470560.1:n.169-67T=
ENST00000607161.5:c.172-67T=	ENSP00000480420.1:n.172-67T=
ENST00000611981.1:n.180-67T=
ENST00000620255.1:n.158-67T=
NM_006331.7:c.169-67T=	NP_006322.4:n.169-67T=
XM_011520907.1:c.169-67T=	XP_011519209.1:n.169-67T=
NM_001320049.1:c.169-67T=	NP_001306978.1:n.169-67T=
NR_135131.1:n.312-67T=
NM_006331.8:c.169-67T= MANE Select	NP_006322.4:n.169-67T=
NM_001320049.2:c.169-67T=	NP_001306978.1:n.169-67T=
NR_135131.2:n.180-67T=