Canonical Allele Identifier: CA2834297

Gene: EVC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5568493C>T , CM000666.2:g.5568493C>T	GRCh38
NC_000004.11:g.5570220C>T , CM000666.1:g.5570220C>T	GRCh37
NC_000004.10:g.5621121C>T	NCBI36
NG_015821.1:g.146056G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_147127.5:c.3508G>A MANE Select	NP_667338.3:p.Ala1170Thr
ENST00000344408.10:c.3508G>A MANE Select	ENSP00000342144.5:p.Ala1170Thr
NM_001166136.1:c.3268G>A	NP_001159608.1:p.Ala1090Thr
NM_001166136.2:c.3268G>A	NP_001159608.1:p.Ala1090Thr
NM_147127.4:c.3508G>A	NP_667338.3:p.Ala1170Thr
ENST00000310917.6:c.3268G>A	ENSP00000311683.2:p.Ala1090Thr
ENST00000344408.9:c.3508G>A	ENSP00000342144.5:p.Ala1170Thr
ENST00000475313.5:c.3268G>A	ENSP00000431981.1:p.Ala1090Thr
ENST00000509670.1:c.*1901G>A	ENSP00000423876.1:n.*1901G>A
XM_011513392.1:c.3517G>A	XP_011511694.1:p.Ala1173Thr
XM_011513393.1:c.3517G>A	XP_011511695.1:p.Ala1173Thr
XM_011513394.1:c.3277G>A	XP_011511696.1:p.Ala1093Thr
XM_017007736.1:c.3268G>A	XP_016863225.1:p.Ala1090Thr
XM_017007737.1:c.3268G>A	XP_016863226.1:p.Ala1090Thr
XM_017007739.1:c.1828G>A	XP_016863228.1:p.Ala610Thr
XM_024453893.1:c.1828G>A	XP_024309661.1:p.Ala610Thr
XR_001741141.1:n.3358G>A