Canonical Allele Identifier: CA356143539

Gene: EVC2

Linked Data

• MyVariant Identifiers: chr4:g.5620345G>C (hg19) ; chr4:g.5618618G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5618618G>C , CM000666.2:g.5618618G>C	GRCh38
NC_000004.11:g.5620345G>C , CM000666.1:g.5620345G>C	GRCh37
NC_000004.10:g.5671246G>C	NCBI36
NG_015821.1:g.95931C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344408.10:c.2566C>G MANE Select	ENSP00000342144.5:p.His856Asp
ENST00000310917.6:c.2326C>G	ENSP00000311683.2:p.His776Asp
ENST00000344408.9:c.2566C>G	ENSP00000342144.5:p.His856Asp
ENST00000475313.5:c.2326C>G	ENSP00000431981.1:p.His776Asp
ENST00000509670.1:c.*959C>G	ENSP00000423876.1:n.*959C>G
NM_001166136.1:c.2326C>G	NP_001159608.1:p.His776Asp
NM_147127.4:c.2566C>G	NP_667338.3:p.His856Asp
XM_011513392.1:c.2575C>G	XP_011511694.1:p.His859Asp
XM_011513393.1:c.2575C>G	XP_011511695.1:p.His859Asp
XM_011513394.1:c.2335C>G	XP_011511696.1:p.His779Asp
XM_017007736.1:c.2326C>G	XP_016863225.1:p.His776Asp
XM_017007737.1:c.2326C>G	XP_016863226.1:p.His776Asp
XM_017007738.1:c.2566C>G	XP_016863227.1:p.His856Asp
XM_017007739.1:c.886C>G	XP_016863228.1:p.His296Asp
XM_024453893.1:c.886C>G	XP_024309661.1:p.His296Asp
XR_001741141.1:n.2631C>G
NM_147127.5:c.2566C>G MANE Select	NP_667338.3:p.His856Asp
NM_001166136.2:c.2326C>G	NP_001159608.1:p.His776Asp