Canonical Allele Identifier: CA356146370

Gene: EVC2

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5562924G>C , CM000666.2:g.5562924G>C	GRCh38
NC_000004.11:g.5564651G>C , CM000666.1:g.5564651G>C	GRCh37
NC_000004.10:g.5615552G>C	NCBI36
NG_015821.1:g.151625C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344408.10:c.3851C>G MANE Select	ENSP00000342144.5:p.Ser1284Ter
ENST00000310917.6:c.3611C>G	ENSP00000311683.2:p.Ser1204Ter
ENST00000344408.9:c.3851C>G	ENSP00000342144.5:p.Ser1284Ter
ENST00000475313.5:c.3419+2334C>G	ENSP00000431981.1:n.3419+2334C>G
ENST00000509670.1:c.*2244C>G	ENSP00000423876.1:n.*2244C>G
NM_001166136.1:c.3611C>G	NP_001159608.1:p.Ser1204Ter
NM_147127.4:c.3851C>G	NP_667338.3:p.Ser1284Ter
XM_011513392.1:c.3860C>G	XP_011511694.1:p.Ser1287Ter
XM_011513393.1:c.3668+2334C>G	XP_011511695.1:n.3668+2334C>G
XM_011513394.1:c.3620C>G	XP_011511696.1:p.Ser1207Ter
XM_017007736.1:c.3611C>G	XP_016863225.1:p.Ser1204Ter
XM_017007737.1:c.3611C>G	XP_016863226.1:p.Ser1204Ter
XM_017007739.1:c.2171C>G	XP_016863228.1:p.Ser724Ter
XM_024453893.1:c.2171C>G	XP_024309661.1:p.Ser724Ter
XR_001741141.1:n.3701C>G
NM_147127.5:c.3851C>G MANE Select	NP_667338.3:p.Ser1284Ter
NM_001166136.2:c.3611C>G	NP_001159608.1:p.Ser1204Ter