Canonical Allele Identifier: CA1435421469

Gene: EVC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5618478C= , CM000666.2:g.5618478C=	GRCh38
NC_000004.11:g.5620205C= , CM000666.1:g.5620205C=	GRCh37
NC_000004.10:g.5671106C=	NCBI36
NG_015821.1:g.96071G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000344408.10:c.2706G= MANE Select	ENSP00000342144.5:p.Gln902=
ENST00000310917.6:c.2466G=	ENSP00000311683.2:p.Gln822=
ENST00000344408.9:c.2706G=	ENSP00000342144.5:p.Gln902=
ENST00000475313.5:c.2466G=	ENSP00000431981.1:p.Gln822=
ENST00000509670.1:c.*1099G=	ENSP00000423876.1:n.*1099G=
NM_001166136.1:c.2466G=	NP_001159608.1:p.Gln822=
NM_147127.4:c.2706G=	NP_667338.3:p.Gln902=
XM_011513392.1:c.2715G=	XP_011511694.1:p.Gln905=
XM_011513393.1:c.2715G=	XP_011511695.1:p.Gln905=
XM_011513394.1:c.2475G=	XP_011511696.1:p.Gln825=
XM_017007736.1:c.2466G=	XP_016863225.1:p.Gln822=
XM_017007737.1:c.2466G=	XP_016863226.1:p.Gln822=
XM_017007738.1:c.2706G=	XP_016863227.1:p.Gln902=
XM_017007739.1:c.1026G=	XP_016863228.1:p.Gln342=
XM_024453893.1:c.1026G=	XP_024309661.1:p.Gln342=
XR_001741141.1:n.2771G=
NM_147127.5:c.2706G= MANE Select	NP_667338.3:p.Gln902=
NM_001166136.2:c.2466G=	NP_001159608.1:p.Gln822=