Canonical Allele Identifier: CA1435421813

Gene: EVC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5618679C= , CM000666.2:g.5618679C=	GRCh38
NC_000004.11:g.5620406C= , CM000666.1:g.5620406C=	GRCh37
NC_000004.10:g.5671307C=	NCBI36
NG_015821.1:g.95870G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344408.10:c.2505G= MANE Select	ENSP00000342144.5:p.Lys835=
ENST00000310917.6:c.2265G=	ENSP00000311683.2:p.Lys755=
ENST00000344408.9:c.2505G=	ENSP00000342144.5:p.Lys835=
ENST00000475313.5:c.2265G=	ENSP00000431981.1:p.Lys755=
ENST00000509670.1:c.*898G=	ENSP00000423876.1:n.*898G=
NM_001166136.1:c.2265G=	NP_001159608.1:p.Lys755=
NM_147127.4:c.2505G=	NP_667338.3:p.Lys835=
XM_011513392.1:c.2514G=	XP_011511694.1:p.Lys838=
XM_011513393.1:c.2514G=	XP_011511695.1:p.Lys838=
XM_011513394.1:c.2274G=	XP_011511696.1:p.Lys758=
XM_017007736.1:c.2265G=	XP_016863225.1:p.Lys755=
XM_017007737.1:c.2265G=	XP_016863226.1:p.Lys755=
XM_017007738.1:c.2505G=	XP_016863227.1:p.Lys835=
XM_017007739.1:c.825G=	XP_016863228.1:p.Lys275=
XM_024453893.1:c.825G=	XP_024309661.1:p.Lys275=
XR_001741141.1:n.2570G=
NM_147127.5:c.2505G= MANE Select	NP_667338.3:p.Lys835=
NM_001166136.2:c.2265G=	NP_001159608.1:p.Lys755=