Canonical Allele Identifier: CA1435421662

Gene: EVC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5618575T= , CM000666.2:g.5618575T=	GRCh38
NC_000004.11:g.5620302T= , CM000666.1:g.5620302T=	GRCh37
NC_000004.10:g.5671203T=	NCBI36
NG_015821.1:g.95974A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344408.10:c.2609A= MANE Select	ENSP00000342144.5:p.Lys870=
ENST00000310917.6:c.2369A=	ENSP00000311683.2:p.Lys790=
ENST00000344408.9:c.2609A=	ENSP00000342144.5:p.Lys870=
ENST00000475313.5:c.2369A=	ENSP00000431981.1:p.Lys790=
ENST00000509670.1:c.*1002A=	ENSP00000423876.1:n.*1002A=
NM_001166136.1:c.2369A=	NP_001159608.1:p.Lys790=
NM_147127.4:c.2609A=	NP_667338.3:p.Lys870=
XM_011513392.1:c.2618A=	XP_011511694.1:p.Lys873=
XM_011513393.1:c.2618A=	XP_011511695.1:p.Lys873=
XM_011513394.1:c.2378A=	XP_011511696.1:p.Lys793=
XM_017007736.1:c.2369A=	XP_016863225.1:p.Lys790=
XM_017007737.1:c.2369A=	XP_016863226.1:p.Lys790=
XM_017007738.1:c.2609A=	XP_016863227.1:p.Lys870=
XM_017007739.1:c.929A=	XP_016863228.1:p.Lys310=
XM_024453893.1:c.929A=	XP_024309661.1:p.Lys310=
XR_001741141.1:n.2674A=
NM_147127.5:c.2609A= MANE Select	NP_667338.3:p.Lys870=
NM_001166136.2:c.2369A=	NP_001159608.1:p.Lys790=