Canonical Allele Identifier: CA2669800480

Gene: EVC2

Linked Data

• gnomAD v4: 4-5618717-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5618717G>T , CM000666.2:g.5618717G>T	GRCh38
NC_000004.11:g.5620444G>T , CM000666.1:g.5620444G>T	GRCh37
NC_000004.10:g.5671345G>T	NCBI36
NG_015821.1:g.95832C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344408.10:c.2502-35C>A MANE Select	ENSP00000342144.5:n.2502-35C>A
ENST00000310917.6:c.2262-35C>A	ENSP00000311683.2:n.2262-35C>A
ENST00000344408.9:c.2502-35C>A	ENSP00000342144.5:n.2502-35C>A
ENST00000475313.5:c.2262-35C>A	ENSP00000431981.1:n.2262-35C>A
ENST00000509670.1:c.*895-35C>A	ENSP00000423876.1:n.*895-35C>A
NM_001166136.1:c.2262-35C>A	NP_001159608.1:n.2262-35C>A
NM_147127.4:c.2502-35C>A	NP_667338.3:n.2502-35C>A
XM_011513392.1:c.2511-35C>A	XP_011511694.1:n.2511-35C>A
XM_011513393.1:c.2511-35C>A	XP_011511695.1:n.2511-35C>A
XM_011513394.1:c.2271-35C>A	XP_011511696.1:n.2271-35C>A
XM_017007736.1:c.2262-35C>A	XP_016863225.1:n.2262-35C>A
XM_017007737.1:c.2262-35C>A	XP_016863226.1:n.2262-35C>A
XM_017007738.1:c.2502-35C>A	XP_016863227.1:n.2502-35C>A
XM_017007739.1:c.822-35C>A	XP_016863228.1:n.822-35C>A
XM_024453893.1:c.822-35C>A	XP_024309661.1:n.822-35C>A
XR_001741141.1:n.2567-35C>A
NM_147127.5:c.2502-35C>A MANE Select	NP_667338.3:n.2502-35C>A
NM_001166136.2:c.2262-35C>A	NP_001159608.1:n.2262-35C>A