Canonical Allele Identifier: CA2834748

Gene: EVC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5622695G>A , CM000666.2:g.5622695G>A	GRCh38
NC_000004.11:g.5624422G>A , CM000666.1:g.5624422G>A	GRCh37
NC_000004.10:g.5675323G>A	NCBI36
NG_015821.1:g.91854C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_147127.5:c.2343C>T MANE Select	NP_667338.3:p.Gly781=
ENST00000344408.10:c.2343C>T MANE Select	ENSP00000342144.5:p.Gly781=
NM_001166136.1:c.2103C>T	NP_001159608.1:p.Gly701=
NM_001166136.2:c.2103C>T	NP_001159608.1:p.Gly701=
NM_147127.4:c.2343C>T	NP_667338.3:p.Gly781=
ENST00000310917.6:c.2103C>T	ENSP00000311683.2:p.Gly701=
ENST00000344408.9:c.2343C>T	ENSP00000342144.5:p.Gly781=
ENST00000475313.5:c.2103C>T	ENSP00000431981.1:p.Gly701=
ENST00000509670.1:c.*736C>T	ENSP00000423876.1:n.*736C>T
XM_011513392.1:c.2352C>T	XP_011511694.1:p.Gly784=
XM_011513393.1:c.2352C>T	XP_011511695.1:p.Gly784=
XM_011513394.1:c.2112C>T	XP_011511696.1:p.Gly704=
XM_017007736.1:c.2103C>T	XP_016863225.1:p.Gly701=
XM_017007737.1:c.2103C>T	XP_016863226.1:p.Gly701=
XM_017007738.1:c.2343C>T	XP_016863227.1:p.Gly781=
XM_017007739.1:c.663C>T	XP_016863228.1:p.Gly221=
XM_024453893.1:c.663C>T	XP_024309661.1:p.Gly221=
XR_001741141.1:n.2408C>T