Canonical Allele Identifier: CA2014342578

Gene: EMG1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6974430T= , CM000674.2:g.6974430T=	GRCh38
NC_000012.11:g.7083592T= , CM000674.1:g.7083592T=	GRCh37
NC_000012.10:g.6953853T=	NCBI36
NG_021408.1:g.8650T=
NG_021408.2:g.8650T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000599672.6:c.260T= MANE Select	ENSP00000470560.1:p.Ile87=
ENST00000261406.7:c.242T=	ENSP00000476966.2:p.Ile81=
ENST00000539196.2:c.123T=
ENST00000599672.5:c.260T=	ENSP00000470560.1:p.Ile87=
ENST00000607161.5:c.263T=	ENSP00000480420.1:p.Ile88=
ENST00000611981.1:n.271T=
ENST00000620255.1:n.249T=
NM_006331.7:c.260T=	NP_006322.4:p.Ile87=
XM_011520907.1:c.260T=	XP_011519209.1:p.Ile87=
NM_001320049.1:c.260T=	NP_001306978.1:p.Ile87=
NR_135131.1:n.403T=
NM_006331.8:c.260T= MANE Select	NP_006322.4:p.Ile87=
NM_001320049.2:c.260T=	NP_001306978.1:p.Ile87=
NR_135131.2:n.271T=