Canonical Allele Identifier: CA3152114

Gene: TRAPPC11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183693055A>C , CM000666.2:g.183693055A>C	GRCh38
NC_000004.11:g.184614208A>C , CM000666.1:g.184614208A>C	GRCh37
NC_000004.10:g.184851202A>C	NCBI36
NG_033102.1:g.38789A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_021942.6:c.2145A>C MANE Select	NP_068761.4:p.Glu715Asp
ENST00000334690.11:c.2145A>C MANE Select	ENSP00000335371.6:p.Glu715Asp
NM_021942.5:c.2145A>C	NP_068761.4:p.Glu715Asp
NM_199053.2:c.2145A>C	NP_951008.1:p.Glu715Asp
NM_199053.3:c.2145A>C	NP_951008.1:p.Glu715Asp
ENST00000334690.10:c.2145A>C	ENSP00000335371.6:p.Glu715Asp
ENST00000357207.8:c.2145A>C	ENSP00000349738.4:p.Glu715Asp
ENST00000505676.5:c.*259A>C	ENSP00000422915.1:n.*259A>C
ENST00000512476.1:c.963A>C	ENSP00000421004.1:p.Glu321Asp
XM_011532180.1:c.2145A>C	XP_011530482.1:p.Glu715Asp
XM_017008537.2:c.2145A>C	XP_016864026.1:p.Glu715Asp
XM_017008538.2:c.2145A>C	XP_016864027.1:p.Glu715Asp
XM_024454179.1:c.2145A>C	XP_024309947.1:p.Glu715Asp
XM_024454180.1:c.2145A>C	XP_024309948.1:p.Glu715Asp
XM_024454181.1:c.795A>C	XP_024309949.1:p.Glu265Asp
XR_001741315.2:n.2337A>C