Canonical Allele Identifier: CA1435421800

Gene: EVC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5618667T= , CM000666.2:g.5618667T=	GRCh38
NC_000004.11:g.5620394T= , CM000666.1:g.5620394T=	GRCh37
NC_000004.10:g.5671295T=	NCBI36
NG_015821.1:g.95882A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344408.10:c.2517A= MANE Select	ENSP00000342144.5:p.Ser839=
ENST00000310917.6:c.2277A=	ENSP00000311683.2:p.Ser759=
ENST00000344408.9:c.2517A=	ENSP00000342144.5:p.Ser839=
ENST00000475313.5:c.2277A=	ENSP00000431981.1:p.Ser759=
ENST00000509670.1:c.*910A=	ENSP00000423876.1:n.*910A=
NM_001166136.1:c.2277A=	NP_001159608.1:p.Ser759=
NM_147127.4:c.2517A=	NP_667338.3:p.Ser839=
XM_011513392.1:c.2526A=	XP_011511694.1:p.Ser842=
XM_011513393.1:c.2526A=	XP_011511695.1:p.Ser842=
XM_011513394.1:c.2286A=	XP_011511696.1:p.Ser762=
XM_017007736.1:c.2277A=	XP_016863225.1:p.Ser759=
XM_017007737.1:c.2277A=	XP_016863226.1:p.Ser759=
XM_017007738.1:c.2517A=	XP_016863227.1:p.Ser839=
XM_017007739.1:c.837A=	XP_016863228.1:p.Ser279=
XM_024453893.1:c.837A=	XP_024309661.1:p.Ser279=
XR_001741141.1:n.2582A=
NM_147127.5:c.2517A= MANE Select	NP_667338.3:p.Ser839=
NM_001166136.2:c.2277A=	NP_001159608.1:p.Ser759=