Canonical Allele Identifier: CA1435421871

Gene: EVC2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5618738_5618739delinsTG , CM000666.2:g.5618738_5618739delinsTG	GRCh38
NC_000004.11:g.5620465_5620466delinsTG , CM000666.1:g.5620465_5620466delinsTG	GRCh37
NC_000004.10:g.5671366_5671367delinsTG	NCBI36
NG_015821.1:g.95810_95811delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344408.10:c.2502-57_2502-56delinsCA MANE Select	ENSP00000342144.5:n.2502-57_2502-56delinsCA
ENST00000310917.6:c.2262-57_2262-56delinsCA	ENSP00000311683.2:n.2262-57_2262-56delinsCA
ENST00000344408.9:c.2502-57_2502-56delinsCA	ENSP00000342144.5:n.2502-57_2502-56delinsCA
ENST00000475313.5:c.2262-57_2262-56delinsCA	ENSP00000431981.1:n.2262-57_2262-56delinsCA
ENST00000509670.1:c.*895-57_*895-56delinsCA	ENSP00000423876.1:n.*895-57_*895-56delinsCA
NM_001166136.1:c.2262-57_2262-56delinsCA	NP_001159608.1:n.2262-57_2262-56delinsCA
NM_147127.4:c.2502-57_2502-56delinsCA	NP_667338.3:n.2502-57_2502-56delinsCA
XM_011513392.1:c.2511-57_2511-56delinsCA	XP_011511694.1:n.2511-57_2511-56delinsCA
XM_011513393.1:c.2511-57_2511-56delinsCA	XP_011511695.1:n.2511-57_2511-56delinsCA
XM_011513394.1:c.2271-57_2271-56delinsCA	XP_011511696.1:n.2271-57_2271-56delinsCA
XM_017007736.1:c.2262-57_2262-56delinsCA	XP_016863225.1:n.2262-57_2262-56delinsCA
XM_017007737.1:c.2262-57_2262-56delinsCA	XP_016863226.1:n.2262-57_2262-56delinsCA
XM_017007738.1:c.2502-57_2502-56delinsCA	XP_016863227.1:n.2502-57_2502-56delinsCA
XM_017007739.1:c.822-57_822-56delinsCA	XP_016863228.1:n.822-57_822-56delinsCA
XM_024453893.1:c.822-57_822-56delinsCA	XP_024309661.1:n.822-57_822-56delinsCA
XR_001741141.1:n.2567-57_2567-56delinsCA
NM_147127.5:c.2502-57_2502-56delinsCA MANE Select	NP_667338.3:n.2502-57_2502-56delinsCA
NM_001166136.2:c.2262-57_2262-56delinsCA	NP_001159608.1:n.2262-57_2262-56delinsCA