Canonical Allele Identifier: CA10651723

Gene: TRAPPC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.13714014C>G , CM000685.2:g.13714014C>G	GRCh38
NC_000023.10:g.13732133C>G , CM000685.1:g.13732133C>G	GRCh37
NC_000023.9:g.13642054C>G	NCBI36
NG_011555.1:g.25610G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001011658.4:c.*393G>C MANE Select	NP_001011658.1:n.*393G>C
ENST00000380579.6:c.*393G>C MANE Select	ENSP00000369953.1:n.*393G>C
NM_001011658.3:c.*393G>C	NP_001011658.1:n.*393G>C
NM_001128835.2:c.*393G>C	NP_001122307.2:n.*393G>C
NM_001128835.3:c.*393G>C	NP_001122307.2:n.*393G>C
NM_014563.5:c.*393G>C	NP_055378.1:n.*393G>C
NM_014563.6:c.*393G>C	NP_055378.1:n.*393G>C
ENST00000359680.9:c.*393G>C	ENSP00000352708.5:n.*393G>C
ENST00000380579.5:c.*393G>C	ENSP00000369953.1:n.*393G>C
ENST00000683569.1:c.*393G>C	ENSP00000508155.1:n.*393G>C
ENST00000683983.1:c.*393G>C	ENSP00000507474.1:n.*393G>C
XM_011545565.1:c.*393G>C	XP_011543867.1:n.*393G>C
XM_011545566.1:c.*393G>C	XP_011543868.1:n.*393G>C
XM_011545566.2:c.*393G>C	XP_011543868.1:n.*393G>C