Canonical Allele Identifier: CA2669800452

Gene: EVC2

Linked Data

• gnomAD v4: 4-5618464-CAGGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5618465_5618468del , CM000666.2:g.5618465_5618468del	GRCh38
NC_000004.11:g.5620192_5620195del , CM000666.1:g.5620192_5620195del	GRCh37
NC_000004.10:g.5671093_5671096del	NCBI36
NG_015821.1:g.96081_96084del

Transcript Alleles

HGVS	Amino-acid change
ENST00000344408.10:c.2706+10_2706+13del MANE Select	ENSP00000342144.5:n.2706+10_2706+13del
ENST00000310917.6:c.2466+10_2466+13del	ENSP00000311683.2:n.2466+10_2466+13del
ENST00000344408.9:c.2706+10_2706+13del	ENSP00000342144.5:n.2706+10_2706+13del
ENST00000475313.5:c.2466+10_2466+13del	ENSP00000431981.1:n.2466+10_2466+13del
ENST00000509670.1:c.*1099+10_*1099+13del	ENSP00000423876.1:n.*1099+10_*1099+13del
NM_001166136.1:c.2466+10_2466+13del	NP_001159608.1:n.2466+10_2466+13del
NM_147127.4:c.2706+10_2706+13del	NP_667338.3:n.2706+10_2706+13del
XM_011513392.1:c.2715+10_2715+13del	XP_011511694.1:n.2715+10_2715+13del
XM_011513393.1:c.2715+10_2715+13del	XP_011511695.1:n.2715+10_2715+13del
XM_011513394.1:c.2475+10_2475+13del	XP_011511696.1:n.2475+10_2475+13del
XM_017007736.1:c.2466+10_2466+13del	XP_016863225.1:n.2466+10_2466+13del
XM_017007737.1:c.2466+10_2466+13del	XP_016863226.1:n.2466+10_2466+13del
XM_017007738.1:c.2706+10_2706+13del	XP_016863227.1:n.2706+10_2706+13del
XM_017007739.1:c.1026+10_1026+13del	XP_016863228.1:n.1026+10_1026+13del
XM_024453893.1:c.1026+10_1026+13del	XP_024309661.1:n.1026+10_1026+13del
XR_001741141.1:n.2771+10_2771+13del
NM_147127.5:c.2706+10_2706+13del MANE Select	NP_667338.3:n.2706+10_2706+13del
NM_001166136.2:c.2466+10_2466+13del	NP_001159608.1:n.2466+10_2466+13del