Canonical Allele Identifier: CA358858667

Gene: TRAPPC11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183664072G>C , CM000666.2:g.183664072G>C	GRCh38
NC_000004.11:g.184585225G>C , CM000666.1:g.184585225G>C	GRCh37
NC_000004.10:g.184822219G>C	NCBI36
NG_033102.1:g.9806G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_021942.6:c.204+1G>C MANE Select	NP_068761.4:n.204+1G>C
ENST00000334690.11:c.204+1G>C MANE Select	ENSP00000335371.6:n.204+1G>C
NM_021942.5:c.204+1G>C	NP_068761.4:n.204+1G>C
NM_199053.2:c.204+1G>C	NP_951008.1:n.204+1G>C
NM_199053.3:c.204+1G>C	NP_951008.1:n.204+1G>C
ENST00000334690.10:c.204+1G>C	ENSP00000335371.6:n.204+1G>C
ENST00000357207.8:c.204+1G>C	ENSP00000349738.4:n.204+1G>C
ENST00000504526.1:n.350+1G>C
ENST00000505676.5:c.162+43G>C	ENSP00000422915.1:n.162+43G>C
ENST00000509857.5:n.55+1G>C
XM_011532180.1:c.204+1G>C	XP_011530482.1:n.204+1G>C
XM_017008537.2:c.204+1G>C	XP_016864026.1:n.204+1G>C
XM_017008538.2:c.204+1G>C	XP_016864027.1:n.204+1G>C
XM_024454179.1:c.204+1G>C	XP_024309947.1:n.204+1G>C
XM_024454180.1:c.204+1G>C	XP_024309948.1:n.204+1G>C
XM_024454181.1:c.-1053+1G>C	XP_024309949.1:n.-1053+1G>C
XR_001741315.2:n.396+1G>C