Canonical Allele Identifier: CA1435421332
Gene: EVC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.5618356G= , CM000666.2:g.5618356G= GRCh38
NC_000004.11:g.5620083G= , CM000666.1:g.5620083G= GRCh37
NC_000004.10:g.5670984G= NCBI36
NG_015821.1:g.96193C=

Transcript Alleles

HGVS Amino-acid change
ENST00000344408.10:c.2706+122C= MANE Select ENSP00000342144.5:n.2706+122C=
ENST00000310917.6:c.2466+122C= ENSP00000311683.2:n.2466+122C=
ENST00000344408.9:c.2706+122C= ENSP00000342144.5:n.2706+122C=
ENST00000475313.5:c.2466+122C= ENSP00000431981.1:n.2466+122C=
ENST00000509670.1:c.*1099+122C= ENSP00000423876.1:n.*1099+122C=
NM_001166136.1:c.2466+122C= NP_001159608.1:n.2466+122C=
NM_147127.4:c.2706+122C= NP_667338.3:n.2706+122C=
XM_011513392.1:c.2715+122C= XP_011511694.1:n.2715+122C=
XM_011513393.1:c.2715+122C= XP_011511695.1:n.2715+122C=
XM_011513394.1:c.2475+122C= XP_011511696.1:n.2475+122C=
XM_017007736.1:c.2466+122C= XP_016863225.1:n.2466+122C=
XM_017007737.1:c.2466+122C= XP_016863226.1:n.2466+122C=
XM_017007738.1:c.2706+122C= XP_016863227.1:n.2706+122C=
XM_017007739.1:c.1026+122C= XP_016863228.1:n.1026+122C=
XM_024453893.1:c.1026+122C= XP_024309661.1:n.1026+122C=
XR_001741141.1:n.2771+122C=
NM_147127.5:c.2706+122C= MANE Select NP_667338.3:n.2706+122C=
NM_001166136.2:c.2466+122C= NP_001159608.1:n.2466+122C=