Canonical Allele Identifier: CA356143532

Gene: EVC2

Linked Data

• MyVariant Identifiers: chr4:g.5620342C>G (hg19) ; chr4:g.5618615C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5618615C>G , CM000666.2:g.5618615C>G	GRCh38
NC_000004.11:g.5620342C>G , CM000666.1:g.5620342C>G	GRCh37
NC_000004.10:g.5671243C>G	NCBI36
NG_015821.1:g.95934G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344408.10:c.2569G>C MANE Select	ENSP00000342144.5:p.Gly857Arg
ENST00000310917.6:c.2329G>C	ENSP00000311683.2:p.Gly777Arg
ENST00000344408.9:c.2569G>C	ENSP00000342144.5:p.Gly857Arg
ENST00000475313.5:c.2329G>C	ENSP00000431981.1:p.Gly777Arg
ENST00000509670.1:c.*962G>C	ENSP00000423876.1:n.*962G>C
NM_001166136.1:c.2329G>C	NP_001159608.1:p.Gly777Arg
NM_147127.4:c.2569G>C	NP_667338.3:p.Gly857Arg
XM_011513392.1:c.2578G>C	XP_011511694.1:p.Gly860Arg
XM_011513393.1:c.2578G>C	XP_011511695.1:p.Gly860Arg
XM_011513394.1:c.2338G>C	XP_011511696.1:p.Gly780Arg
XM_017007736.1:c.2329G>C	XP_016863225.1:p.Gly777Arg
XM_017007737.1:c.2329G>C	XP_016863226.1:p.Gly777Arg
XM_017007738.1:c.2569G>C	XP_016863227.1:p.Gly857Arg
XM_017007739.1:c.889G>C	XP_016863228.1:p.Gly297Arg
XM_024453893.1:c.889G>C	XP_024309661.1:p.Gly297Arg
XR_001741141.1:n.2634G>C
NM_147127.5:c.2569G>C MANE Select	NP_667338.3:p.Gly857Arg
NM_001166136.2:c.2329G>C	NP_001159608.1:p.Gly777Arg