Canonical Allele Identifier: CA326090701

Gene: TRAPPC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.13713698G>C , CM000685.2:g.13713698G>C	GRCh38
NC_000023.10:g.13731817G>C , CM000685.1:g.13731817G>C	GRCh37
NC_000023.9:g.13641738G>C	NCBI36
NG_011555.1:g.25926C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683569.1:c.*709C>G	ENSP00000508155.1:n.*709C>G
ENST00000683983.1:c.*709C>G	ENSP00000507474.1:n.*709C>G
ENST00000380579.6:c.*709C>G MANE Select	ENSP00000369953.1:n.*709C>G
ENST00000359680.9:c.*709C>G	ENSP00000352708.5:n.*709C>G
ENST00000380579.5:c.*709C>G	ENSP00000369953.1:n.*709C>G
NM_001011658.3:c.*709C>G	NP_001011658.1:n.*709C>G
NM_001128835.2:c.*709C>G	NP_001122307.2:n.*709C>G
NM_014563.5:c.*709C>G	NP_055378.1:n.*709C>G
XM_011545565.1:c.*709C>G	XP_011543867.1:n.*709C>G
XM_011545566.1:c.*709C>G	XP_011543868.1:n.*709C>G
XM_011545566.2:c.*709C>G	XP_011543868.1:n.*709C>G
NM_001011658.4:c.*709C>G MANE Select	NP_001011658.1:n.*709C>G
NM_001128835.3:c.*709C>G	NP_001122307.2:n.*709C>G
NM_014563.6:c.*709C>G	NP_055378.1:n.*709C>G