Canonical Allele Identifier: CA10653808

Gene: TRAPPC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.13714140_13714141insA , CM000685.2:g.13714140_13714141insA	GRCh38
NC_000023.10:g.13732259_13732260insA , CM000685.1:g.13732259_13732260insA	GRCh37
NC_000023.9:g.13642180_13642181insA	NCBI36
NG_011555.1:g.25483_25484insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683569.1:c.*266_*267insT	ENSP00000508155.1:n.*266_*267insT
ENST00000683983.1:c.*266_*267insT	ENSP00000507474.1:n.*266_*267insT
ENST00000380579.6:c.*266_*267insT MANE Select	ENSP00000369953.1:n.*266_*267insT
ENST00000359680.9:c.*266_*267insT	ENSP00000352708.5:n.*266_*267insT
ENST00000380579.5:c.*266_*267insT	ENSP00000369953.1:n.*266_*267insT
NM_001011658.3:c.*266_*267insT	NP_001011658.1:n.*266_*267insT
NM_001128835.2:c.*266_*267insT	NP_001122307.2:n.*266_*267insT
NM_014563.5:c.*266_*267insT	NP_055378.1:n.*266_*267insT
XM_011545565.1:c.*266_*267insT	XP_011543867.1:n.*266_*267insT
XM_011545566.1:c.*266_*267insT	XP_011543868.1:n.*266_*267insT
XM_011545566.2:c.*266_*267insT	XP_011543868.1:n.*266_*267insT
NM_001011658.4:c.*266_*267insT MANE Select	NP_001011658.1:n.*266_*267insT
NM_001128835.3:c.*266_*267insT	NP_001122307.2:n.*266_*267insT
NM_014563.6:c.*266_*267insT	NP_055378.1:n.*266_*267insT