Canonical Allele Identifier: CA356143568
Gene: EVC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.5618630T>C , CM000666.2:g.5618630T>C GRCh38
NC_000004.11:g.5620357T>C , CM000666.1:g.5620357T>C GRCh37
NC_000004.10:g.5671258T>C NCBI36
NG_015821.1:g.95919A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344408.10:c.2554A>G MANE Select ENSP00000342144.5:p.Arg852Gly
ENST00000310917.6:c.2314A>G ENSP00000311683.2:p.Arg772Gly
ENST00000344408.9:c.2554A>G ENSP00000342144.5:p.Arg852Gly
ENST00000475313.5:c.2314A>G ENSP00000431981.1:p.Arg772Gly
ENST00000509670.1:c.*947A>G ENSP00000423876.1:n.*947A>G
NM_001166136.1:c.2314A>G NP_001159608.1:p.Arg772Gly
NM_147127.4:c.2554A>G NP_667338.3:p.Arg852Gly
XM_011513392.1:c.2563A>G XP_011511694.1:p.Arg855Gly
XM_011513393.1:c.2563A>G XP_011511695.1:p.Arg855Gly
XM_011513394.1:c.2323A>G XP_011511696.1:p.Arg775Gly
XM_017007736.1:c.2314A>G XP_016863225.1:p.Arg772Gly
XM_017007737.1:c.2314A>G XP_016863226.1:p.Arg772Gly
XM_017007738.1:c.2554A>G XP_016863227.1:p.Arg852Gly
XM_017007739.1:c.874A>G XP_016863228.1:p.Arg292Gly
XM_024453893.1:c.874A>G XP_024309661.1:p.Arg292Gly
XR_001741141.1:n.2619A>G
NM_147127.5:c.2554A>G MANE Select NP_667338.3:p.Arg852Gly
NM_001166136.2:c.2314A>G NP_001159608.1:p.Arg772Gly