Canonical Allele Identifier: CA1435391965

Gene: EVC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5565266T= , CM000666.2:g.5565266T=	GRCh38
NC_000004.11:g.5566993T= , CM000666.1:g.5566993T=	GRCh37
NC_000004.10:g.5617894T=	NCBI36
NG_015821.1:g.149283A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000344408.10:c.3651A= MANE Select	ENSP00000342144.5:p.Arg1217=
ENST00000310917.6:c.3411A=	ENSP00000311683.2:p.Arg1137=
ENST00000344408.9:c.3651A=	ENSP00000342144.5:p.Arg1217=
ENST00000475313.5:c.3411A=	ENSP00000431981.1:p.Arg1137=
ENST00000509670.1:c.*2044A=	ENSP00000423876.1:n.*2044A=
NM_001166136.1:c.3411A=	NP_001159608.1:p.Arg1137=
NM_147127.4:c.3651A=	NP_667338.3:p.Arg1217=
XM_011513392.1:c.3660A=	XP_011511694.1:p.Arg1220=
XM_011513393.1:c.3660A=	XP_011511695.1:p.Arg1220=
XM_011513394.1:c.3420A=	XP_011511696.1:p.Arg1140=
XM_017007736.1:c.3411A=	XP_016863225.1:p.Arg1137=
XM_017007737.1:c.3411A=	XP_016863226.1:p.Arg1137=
XM_017007739.1:c.1971A=	XP_016863228.1:p.Arg657=
XM_024453893.1:c.1971A=	XP_024309661.1:p.Arg657=
XR_001741141.1:n.3501A=
NM_147127.5:c.3651A= MANE Select	NP_667338.3:p.Arg1217=
NM_001166136.2:c.3411A=	NP_001159608.1:p.Arg1137=