Canonical Allele Identifier: CA1435421757

Gene: EVC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5618630T= , CM000666.2:g.5618630T=	GRCh38
NC_000004.11:g.5620357T= , CM000666.1:g.5620357T=	GRCh37
NC_000004.10:g.5671258T=	NCBI36
NG_015821.1:g.95919A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344408.10:c.2554A= MANE Select	ENSP00000342144.5:p.Arg852=
ENST00000310917.6:c.2314A=	ENSP00000311683.2:p.Arg772=
ENST00000344408.9:c.2554A=	ENSP00000342144.5:p.Arg852=
ENST00000475313.5:c.2314A=	ENSP00000431981.1:p.Arg772=
ENST00000509670.1:c.*947A=	ENSP00000423876.1:n.*947A=
NM_001166136.1:c.2314A=	NP_001159608.1:p.Arg772=
NM_147127.4:c.2554A=	NP_667338.3:p.Arg852=
XM_011513392.1:c.2563A=	XP_011511694.1:p.Arg855=
XM_011513393.1:c.2563A=	XP_011511695.1:p.Arg855=
XM_011513394.1:c.2323A=	XP_011511696.1:p.Arg775=
XM_017007736.1:c.2314A=	XP_016863225.1:p.Arg772=
XM_017007737.1:c.2314A=	XP_016863226.1:p.Arg772=
XM_017007738.1:c.2554A=	XP_016863227.1:p.Arg852=
XM_017007739.1:c.874A=	XP_016863228.1:p.Arg292=
XM_024453893.1:c.874A=	XP_024309661.1:p.Arg292=
XR_001741141.1:n.2619A=
NM_147127.5:c.2554A= MANE Select	NP_667338.3:p.Arg852=
NM_001166136.2:c.2314A=	NP_001159608.1:p.Arg772=