Canonical Allele Identifier: CA356146372

Gene: EVC2

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5562925A>T , CM000666.2:g.5562925A>T	GRCh38
NC_000004.11:g.5564652A>T , CM000666.1:g.5564652A>T	GRCh37
NC_000004.10:g.5615553A>T	NCBI36
NG_015821.1:g.151624T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344408.10:c.3850T>A MANE Select	ENSP00000342144.5:p.Ser1284Thr
ENST00000310917.6:c.3610T>A	ENSP00000311683.2:p.Ser1204Thr
ENST00000344408.9:c.3850T>A	ENSP00000342144.5:p.Ser1284Thr
ENST00000475313.5:c.3419+2333T>A	ENSP00000431981.1:n.3419+2333T>A
ENST00000509670.1:c.*2243T>A	ENSP00000423876.1:n.*2243T>A
NM_001166136.1:c.3610T>A	NP_001159608.1:p.Ser1204Thr
NM_147127.4:c.3850T>A	NP_667338.3:p.Ser1284Thr
XM_011513392.1:c.3859T>A	XP_011511694.1:p.Ser1287Thr
XM_011513393.1:c.3668+2333T>A	XP_011511695.1:n.3668+2333T>A
XM_011513394.1:c.3619T>A	XP_011511696.1:p.Ser1207Thr
XM_017007736.1:c.3610T>A	XP_016863225.1:p.Ser1204Thr
XM_017007737.1:c.3610T>A	XP_016863226.1:p.Ser1204Thr
XM_017007739.1:c.2170T>A	XP_016863228.1:p.Ser724Thr
XM_024453893.1:c.2170T>A	XP_024309661.1:p.Ser724Thr
XR_001741141.1:n.3700T>A
NM_147127.5:c.3850T>A MANE Select	NP_667338.3:p.Ser1284Thr
NM_001166136.2:c.3610T>A	NP_001159608.1:p.Ser1204Thr